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The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss

โœ Scribed by Haris Kokotas; Maria Grigoriadou; George S. Korres; Elisabeth Ferekidou; Eleftheria Papadopoulou; Polyxene Neou; Aglaia Giannoulia-Karantana; Dimitrios Kandiloros; Stavros Korres; Michael B. Petersen


Book ID
116299329
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
142 KB
Volume
390
Category
Article
ISSN
0006-291X

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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