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J Med Genet. 2005 Jul;42(7):588-94.

A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment.

PMID:
15994881
PMCID:
PMC1736094
DOI:
10.1136/jmg.2004.028324
[Indexed for MEDLINE]
Free PMC Article

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