New era in genetics of early-onset muscle disease: Breakthroughs and challenges.

Ravenscroft, Gianina; Davis, Mark R; Lamont, Phillipa; Forrest, Alistair; Laing, Nigel G

Ravenscroft, Gianina; Davis, Mark R; Lamont, Phillipa; Forrest, Alistair; Laing, Nigel G.

Afiliación

Ravenscroft G; Harry Perkins Institute of Medical Research and the Centre for Medical Research, University of Western Australia, Nedlands, Australia.
Davis MR; Department of Diagnostic Genomics, Pathwest, QEII Medical Centre, Nedlands, Australia.
Lamont P; Harry Perkins Institute of Medical Research and the Centre for Medical Research, University of Western Australia, Nedlands, Australia; Neurogenetic unit, Dept of Neurology, Royal Perth Hospital and The Perth Children's Hospital, Western Australia, Australia.
Forrest A; Harry Perkins Institute of Medical Research and the Centre for Medical Research, University of Western Australia, Nedlands, Australia.
Laing NG; Harry Perkins Institute of Medical Research and the Centre for Medical Research, University of Western Australia, Nedlands, Australia; Department of Diagnostic Genomics, Pathwest, QEII Medical Centre, Nedlands, Australia. Electronic address: nigel.laing@perkins.uwa.edu.au.

Semin Cell Dev Biol ; 64: 160-170, 2017 04.

Article en En | MEDLINE | ID: mdl-27519468

Asunto(s)

Enfermedades Musculares/genética; Edad de Inicio; Animales; Humanos; Proteínas Musculares/genética

Palabras clave

Congenital muscular dystrophy; Congenital myasthenic syndrome; Congenital myopathy; Genetics; Next generation sequencing

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Musculares Límite: Animals / Humans Idioma: En Revista: Semin Cell Dev Biol Asunto de la revista: EMBRIOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Australia

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