tallózása szerző szerint "Melegh, Béla Imre"

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Erratum to: Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases

Halmainé Komlósi, Katalin; Maász, Anita; Kisfali, Péter; Hadzsiev, Kinga; Bene, Judit; Melegh, Béla Imre; Ablonczy, Mária; Németh, Krisztina; Fekete, György; Melegh, Béla (2013)
Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA^^Ser(UCN)^^^ and Review of Published Cases

Halmainé Komlósi, Katalin; Maász, Anita; Kisfali, Péter; Hadzsiev, Kinga; Bene, Judit; Melegh, Béla Imre; Ablonczy, Mária; Németh, Krisztina; Fekete, György; Melegh, Béla (2013)

The m.7510T>C mitochondrial DNA (mtDNA) mutation is a tRNA(Ser(UCN)) alteration leading to matrilineal isolated hearing impairment. The current paper reviews the available reports on the m.7510T>C mtDNA mutation, with ...

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