[go: up one dir, main page]

Khuller et al., 2021 - Google Patents

MFSD2A-associated primary microcephaly-Expanding the clinical and mutational spectrum of this ultra-rare disease

Khuller et al., 2021

Document ID
8878231319313600408
Author
Khuller K
Yigit G
Grijalva C
Altmueller J
Thiele H
Nürnberg P
Elcioglu N
Yeter B
Hehr U
Stein A
Della Marina A
Koeninger A
Depienne C
Kaiser F
Wollnik B
Kuechler A
Publication year
Publication venue
European Journal of Medical Genetics

External Links

Snippet

MFSD2A, a member of the major facilitator superfamily (MFS), is a transmembrane transporter responsible for the uptake of specific essential fatty acids through the blood-brain barrier (BBB) to the brain. The transporter is crucial for early embryonic brain development …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Hybridisation probes
    • C12Q1/6883Hybridisation probes for diseases caused by alterations of genetic material
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705Receptors; Cell surface antigens; Cell surface determinants
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/156Polymorphic or mutational markers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic, hydroximic acids

Similar Documents

Publication Publication Date Title
US11096956B2 (en) Antisense oligomers and uses thereof
Notaras et al. The BDNF gene Val66Met polymorphism as a modifier of psychiatric disorder susceptibility: progress and controversy
Oláhová et al. LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population
Kara et al. Genetic and phenotypic characterization of complex hereditary spastic paraplegia
Zaharieva et al. Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or ‘classical’congenital myopathy
Balreira et al. ANO10 mutations cause ataxia and coenzyme Q10 deficiency
Hirata et al. ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
Bonora et al. Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy
Feichtinger et al. Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy
Zanni et al. A novel mutation in the endosomal Na+/H+ exchanger NHE6 (SLC9A6) causes Christianson syndrome with electrical status epilepticus during slow-wave sleep (ESES)
Sambuughin et al. Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2
Suleiman et al. WDR45B‐related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: a consistent neurodevelopmental syndrome
Khuller et al. MFSD2A-associated primary microcephaly-Expanding the clinical and mutational spectrum of this ultra-rare disease
Jørgensen et al. Vascular Ehlers–Danlos syndrome in siblings with biallelic COL3A1 sequence variants and marked clinical variability in the extended family
Sheffer et al. Biallelic variants in AGTPBP1, involved in tubulin deglutamylation, are associated with cerebellar degeneration and motor neuropathy
Tabares-Seisdedos et al. Variations in genes regulating neuronal migration predict reduced prefrontal cognition in schizophrenia and bipolar subjects from mediterranean Spain: a preliminary study
Liao et al. SPG35 contributes to the second common subtype of AR‐HSP in China: frequency analysis and functional characterization of FA2H gene mutations
Kaiyrzhanov et al. Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum
De Pace et al. Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics
Kettwig et al. Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review
Guasto et al. Biallelic variants in SLC35B2 cause a novel chondrodysplasia with hypomyelinating leukodystrophy
Ge et al. Recessive mutations in proximal I-band of TTN gene cause severe congenital multi-minicore disease without cardiac involvement
Häusler et al. A novel homozygous splice-site mutation in the SPTBN4 gene causes axonal neuropathy without intellectual disability
Zhao et al. First report of paternal uniparental disomy of chromosome 8 with SLC52A2 mutation in Brown-vialetto-van laere syndrome type 2 and an analysis of genotype-phenotype correlations
Burke et al. Compound heterozygous KCTD7 variants in progressive myoclonus epilepsy