Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.

Bánfai, Zsolt; Hadzsiev, Kinga; Pál, Endre; Komlósi, Katalin; Melegh, Márton; Balikó, László; Melegh, Béla

Bánfai, Zsolt; Hadzsiev, Kinga; Pál, Endre; Komlósi, Katalin; Melegh, Márton; Balikó, László; Melegh, Béla.

Afiliación

Bánfai Z; Department of Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary.
Hadzsiev K; Szentágothai Research Centre, University of Pécs, Ifjúság út 20, Pécs, H-7624, Hungary.
Pál E; Department of Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary.
Komlósi K; Szentágothai Research Centre, University of Pécs, Ifjúság út 20, Pécs, H-7624, Hungary.
Melegh M; Neurology Clinic, University of Pécs, Rét u. 2, Pécs, H-7623, Hungary.
Balikó L; Department of Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary.
Melegh B; Szentágothai Research Centre, University of Pécs, Ifjúság út 20, Pécs, H-7624, Hungary.

BMC Med Genet ; 18(1): 150, 2017 12 16.

Article en En | MEDLINE | ID: mdl-29248012

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: BMC Med Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Hungria

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