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Wang et al., 1995 - Google Patents

Mice lacking ornithine–δ–amino–transferase have paradoxical neonatal hypoornithinaemia and retinal degeneration

Wang et al., 1995

Document ID
317085612656511581
Author
Wang T
Lawler A
Steel G
Sipila I
Milam A
Valle D
Publication year
Publication venue
Nature genetics

External Links

Snippet

Deficiency of ornithine–δ–aminotransferase (OAT) in humans causes hyperornithinaemia and gyrate atrophy (GA), a blinding chorioretinal degeneration. Surprisingly, OAT–deficient mice produced by gene targeting exhibit neonatal hypoornithinaemia and lethality …
Continue reading at www.nature.com (other versions)

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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
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