Učitavanje...
Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin
PURPOSE: It has been demonstrated that mutations in deafness, autosomal recessive 31 (DFNB31), the gene encoding whirlin, is responsible for nonsyndromic hearing loss (NSHL; DFNB31) and Usher syndrome type II (USH2D). We screened DFNB31 in a large cohort of patients with different clinical subtypes...
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| Glavni autori: | , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Molecular Vision
2010
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2845667/ https://ncbi.nlm.nih.gov/pubmed/20352026 |
| Oznake: |
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