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Hereditary hearing loss: From human mutation to mechanism

✍ Scribed by Danielle R. Lenz; Karen B. Avraham


Book ID
116525587
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
923 KB
Volume
281
Category
Article
ISSN
0378-5955

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Hearing loss due to the mitochondrial A1
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Six Italian families with familial nonsyndromic hearing loss consistent with a maternal pattern of inheritance were analyzed for mitochondrial mutations. The three known mitochondrial mutations associated with nonsyndromic hearing loss were investigated by polymerase chain reaction amplification, fo