reference/29611610

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startingPage	1885
bibliographicCitation	Imtiaz F, Taibah K, Bin-Khamis G, Kennedy S, Hemidan A, Al-Qahtani F, Tabbara K, Al Mubarak B, Ramzan K, Meyer BF, Al-Owain M. USH1G with unique retinal findings caused by a novel truncating mutation identified by genome-wide linkage analysis. Mol Vis. 2012;18():1885–94. PMID: 22876113; PMCID: PMC3413430.
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date	2012
identifier	https://pubmed.ncbi.nlm.nih.gov/22876113 https://pubmed.ncbi.nlm.nih.gov/PMC3413430
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/
title	USH1G with unique retinal findings caused by a novel truncating mutation identified by genome-wide linkage analysis
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