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PMCA4 (ATP2B4) mutation in familial spastic paraplegia.
Li, Miaoxin; Ho, Philip Wing-Lok; Pang, Shirley Yin-Yu; Tse, Zero Ho-Man; Kung, Michelle Hiu-Wai; Sham, Pak-Chung; Ho, Shu-Leong.
Afiliação
  • Li M; Department of Psychiatry, University of Hong Kong, Hong Kong, P. R. China; Centre for Reproduction, Development and Growth, University of Hong Kong, Hong Kong, P. R. China; Centre for Genomic Sciences, University of Hong Kong, Hong Kong, P. R. China.
  • Ho PW; Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, P. R. China; Research Centre of Heart, Brain, Hormone and Healthy Aging, University of Hong Kong, Hong Kong, P. R. China.
  • Pang SY; Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, P. R. China.
  • Tse ZH; Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, P. R. China.
  • Kung MH; Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, P. R. China.
  • Sham PC; Department of Psychiatry, University of Hong Kong, Hong Kong, P. R. China; Centre for Reproduction, Development and Growth, University of Hong Kong, Hong Kong, P. R. China; Centre for Genomic Sciences, University of Hong Kong, Hong Kong, P. R. China.
  • Ho SL; Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, P. R. China; Research Centre of Heart, Brain, Hormone and Healthy Aging, University of Hong Kong, Hong Kong, P. R. China.
PLoS One ; 9(8): e104790, 2014.
Article em En | MEDLINE | ID: mdl-25119969

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Paraplegia Espástica Hereditária / Povo Asiático / ATPases Transportadoras de Cálcio da Membrana Plasmática Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Paraplegia Espástica Hereditária / Povo Asiático / ATPases Transportadoras de Cálcio da Membrana Plasmática Idioma: En Ano de publicação: 2014 Tipo de documento: Article