Molecular mechanism of a frequent genetic form of deafness
- PMID: 12917317
- DOI: 10.1056/NEJMc030327
Molecular mechanism of a frequent genetic form of deafness
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A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.N Engl J Med. 2002 Jan 24;346(4):243-9. doi: 10.1056/NEJMoa012052. N Engl J Med. 2002. PMID: 11807148
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