A large cohort study confirming that specific haplotype 4A161PAS is exclusively associated with the Chinese FSHD1.

Lin, F; He, J-J; Lin, X-D; Wang, D-N; Lin, H-X; Liu, X-Y; Lin, M-T; Wang, N; Wang, Z-Q

Lin, F; He, J-J; Lin, X-D; Wang, D-N; Lin, H-X; Liu, X-Y; Lin, M-T; Wang, N; Wang, Z-Q.

Afiliação

Lin F; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fujian, China.
He JJ; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fujian, China.
Lin XD; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fujian, China.
Wang DN; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fujian, China.
Lin HX; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fujian, China.
Liu XY; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fujian, China.
Lin MT; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fujian, China.
Wang N; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fujian, China.
Wang ZQ; Fujian Key Laboratory of Molecular Neurology, Fuzhou, China.

Clin Genet ; 90(6): 558-559, 2016 12.

Article em En | MEDLINE | ID: mdl-27666735

Assuntos

Haplótipos; Distrofia Muscular Facioescapuloumeral/genética; Povo Asiático; Estudos de Coortes; Humanos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Haplótipos / Distrofia Muscular Facioescapuloumeral Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Genet Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China

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