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

Komlósi, Katalin; Maász, Anita; Kisfali, Péter; Hadzsiev, Kinga; Bene, Judit; Melegh, Béla I; Melegh, Béla; Ablonczy, Mária; Németh, Krisztina; Fekete, György

Komlósi, Katalin; Maász, Anita; Kisfali, Péter; Hadzsiev, Kinga; Bene, Judit; Melegh, Béla I; Melegh, Béla; Ablonczy, Mária; Németh, Krisztina; Fekete, György.

Afiliación

Komlósi K; Department of Medical Genetics, University of Pécs, József A. út 7, Pécs, H-7623, Hungary. komlosi.katalin@pte.hu.
Maász A; Department of Medical Genetics, University of Pécs, József A. út 7, Pécs, H-7623, Hungary.
Kisfali P; Department of Medical Genetics, University of Pécs, József A. út 7, Pécs, H-7623, Hungary.
Hadzsiev K; Department of Medical Genetics, University of Pécs, József A. út 7, Pécs, H-7623, Hungary.
Bene J; Department of Medical Genetics, University of Pécs, József A. út 7, Pécs, H-7623, Hungary.
Melegh BI; Department of Medical Genetics, University of Pécs, József A. út 7, Pécs, H-7623, Hungary.
Melegh B; Department of Medical Genetics, University of Pécs, József A. út 7, Pécs, H-7623, Hungary.
Ablonczy M; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Németh K; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Fekete G; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.

JIMD Rep ; 9: 105-111, 2013.

Article en En | MEDLINE | ID: mdl-23430555

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JIMD Rep Año: 2013 Tipo del documento: Article País de afiliación: Hungria