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Volumn 25, Issue 5, 2004, Pages 699-706

Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12)

Author keywords

CDH23 gene; DFNB12; Genotype phenotype correlation; Hearing impairment; Retinitis pigmentosa; USH1D; Usher syndrome

Indexed keywords

CADHERIN; CADHERIN 23; LIPOFUSCIN; UNCLASSIFIED DRUG;

EID: 4544332025     PISSN: 15317129     EISSN: None     Source Type: Journal    
DOI: 10.1097/00129492-200409000-00009     Document Type: Article
Times cited : (30)

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