Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis.

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Citation

Perrault I, Rozet JM, Ghazi I, Leowski C, Bonnemaison M, Gerber S, Ducroq D, Cabot A, Souied E, Dufier JL, Munnich A, Kaplan J

Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis.

Am J Hum Genet. 1999 Apr;64(4):1225-8.

PubMed ID
10090910 [ View in PubMed
]
Abstract

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DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Retinoid isomerohydrolaseQ16518Details