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Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

PaperCitations, authors & open-access status

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23 is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 558 citations, 2001 year and bronze oa status.

558
Citations
2001
Year
bronze
OA Status

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