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Clinical and genetic features of patients with facial-sparing facioscapulohumeral muscular dystrophy.
He, J-J; Lin, X-D; Lin, F; Xu, G-R; Xu, L-Q; Hu, W; Wang, D-N; Lin, H-X; Lin, M-T; Wang, N; Wang, Z-Q.
Affiliation
  • He JJ; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Lin XD; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Lin F; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Xu GR; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Xu LQ; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Hu W; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Wang DN; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Lin HX; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Lin MT; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Wang N; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
  • Wang ZQ; Fujian Key Laboratory of Molecular Neurology, Fuzhou, China.
Eur J Neurol ; 25(2): 356-364, 2018 02.
Article in En | MEDLINE | ID: mdl-29112784
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 4 / Muscular Dystrophy, Facioscapulohumeral Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2018 Document type: Article Affiliation country: China Country of publication: United kingdom
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 4 / Muscular Dystrophy, Facioscapulohumeral Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2018 Document type: Article Affiliation country: China Country of publication: United kingdom