Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia?

Cascalho, Ana; Jacquemyn, Julie; Goodchild, Rose E

Cascalho, Ana; Jacquemyn, Julie; Goodchild, Rose E.

Afiliação

Cascalho A; Vlaams Instituut voor Biotechnologie Centre for the Biology of Disease, Leuven, Belgium.
Jacquemyn J; KU Leuven, Department of Human Genetics, Leuven, Belgium.
Goodchild RE; Vlaams Instituut voor Biotechnologie Centre for the Biology of Disease, Leuven, Belgium.

Mov Disord ; 32(3): 371-381, 2017 03.

Article em En | MEDLINE | ID: mdl-27911022

Assuntos

Distonia Muscular Deformante/metabolismo; Chaperonas Moleculares/metabolismo; Animais; Distonia Muscular Deformante/genética; Humanos; Chaperonas Moleculares/genética

Palavras-chave

dystonia; endoplasmic reticulum; membrane; nuclear envelope; torsinA

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Chaperonas Moleculares / Distonia Muscular Deformante Idioma: En Ano de publicação: 2017 Tipo de documento: Article

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