Your browser doesn't support javascript.
loading
The MFN2 V705I Variant Is Not a Disease-Causing Mutation: A Segregation Analysis in a CMT2 Family.
Albulym, Obaid M; Zhu, Danqing; Reddel, Stephen; Kennerson, Marina; Nicholson, Garth.
Afiliação
  • Albulym OM; Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW 2139, Australia ; Sydney Medical School, University of Sydney, Sydney, NSW 2008, Australia.
  • Zhu D; Molecular Medicine Laboratory, Concord Hospital, Concord, NSW 2139, Australia.
  • Reddel S; Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW 2139, Australia ; Sydney Medical School, University of Sydney, Sydney, NSW 2008, Australia ; Molecular Medicine Laboratory, Concord Hospital, Concord, NSW 2139, Australia.
  • Kennerson M; Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW 2139, Australia ; Sydney Medical School, University of Sydney, Sydney, NSW 2008, Australia ; Molecular Medicine Laboratory, Concord Hospital, Concord, NSW 2139, Australia.
  • Nicholson G; Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW 2139, Australia ; Sydney Medical School, University of Sydney, Sydney, NSW 2008, Australia ; Molecular Medicine Laboratory, Concord Hospital, Concord, NSW 2139, Australia.
J Neurodegener Dis ; 2013: 495873, 2013.
Article em En | MEDLINE | ID: mdl-26316991
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2013 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2013 Tipo de documento: Article