AF180340[Secondary Source ID] - Search Results

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP. Sohocki MM, et al. Nat Genet. 2000 Jan;24(1):79-83. doi: 10.1038/71732. Nat Genet. 2000. PMID: 10615133 Free PMC article.

Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humans.

Sohocki MM, Sullivan LS, Tirpak DL, Daiger SP. Sohocki MM, et al. Mamm Genome. 2001 Jul;12(7):566-8. doi: 10.1007/s003350020024. Mamm Genome. 2001. PMID: 11420621 Free PMC article.

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