Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference25 articles.
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4. Maternally inherited deafness associated with a T1095C mutation in the mtDNA;Tessa;Eur. J. Hum. Genet.,2001
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