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PubMed for id: 393392
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Identification of a novel locus for a USH3 like syndrome combined with congenital cataract.
Clin Genet. 2010 Oct;78(4):388-97. doi: 10.1111/j.1399-0004.2010.01393.x.
Clin Genet. 2010.
PMID: 20236115
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
Ahmed ZM, Riazuddin S, Khan SN, Friedman PL, Riazuddin S, Friedman TB.
Ahmed ZM, et al.
Clin Genet. 2009 Jan;75(1):86-91. doi: 10.1111/j.1399-0004.2008.01038.x. Epub 2008 May 25.
Clin Genet. 2009.
PMID: 18505454
Free PMC article.
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