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A PDGFB mutation causes paroxysmal nonkinesigenic dyskinesia with brain calcification.
Wang, Cheng; Ma, Xixiang; Xu, Xuan; Huang, Benyan; Sun, Hao; Li, Lulu; Zhang, Min; Liu, Jing Yu.
Afiliação
  • Wang C; Key Laboratory of Molecular Biophysics of the Ministry of Education, Center for Human Genome Research, College of Life Science and Technology, Huazhong University of Science and Technology (HUST), Wuhan, China.
  • Ma X; Key Laboratory of Molecular Biophysics of the Ministry of Education, Center for Human Genome Research, College of Life Science and Technology, Huazhong University of Science and Technology (HUST), Wuhan, China.
  • Xu X; Key Laboratory of Molecular Biophysics of the Ministry of Education, Center for Human Genome Research, College of Life Science and Technology, Huazhong University of Science and Technology (HUST), Wuhan, China.
  • Huang B; Department of Neurology, Tongji Hospital of HUST, Wuhan, China.
  • Sun H; Key Laboratory of Molecular Biophysics of the Ministry of Education, Center for Human Genome Research, College of Life Science and Technology, Huazhong University of Science and Technology (HUST), Wuhan, China.
  • Li L; Key Laboratory of Molecular Biophysics of the Ministry of Education, Center for Human Genome Research, College of Life Science and Technology, Huazhong University of Science and Technology (HUST), Wuhan, China.
  • Zhang M; Department of Neurology, Tongji Hospital of HUST, Wuhan, China.
  • Liu JY; Key Laboratory of Molecular Biophysics of the Ministry of Education, Center for Human Genome Research, College of Life Science and Technology, Huazhong University of Science and Technology (HUST), Wuhan, China.
Mov Disord ; 32(7): 1104-1106, 2017 07.
Article em En | MEDLINE | ID: mdl-28556368
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encefalopatias / Calcinose / Coreia / Genes sis / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Adult / Animals / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encefalopatias / Calcinose / Coreia / Genes sis / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Adult / Animals / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article