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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

Publication details
Download http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1736094
Publisher BMJ Group
Repository PubMed Central (PMC3 - NLM DTD) (United States)
Keywords Letter to JMG
Type Text
Language English