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Spectrum of SLC20A2, PDGFRB, PDGFB, and XPR1 mutations in a large cohort of patients with primary familial brain calcification.
Guo, Xin-Xin; Zou, Xiao-Huan; Wang, Chong; Yao, Xiang-Ping; Su, Hui-Zhen; Lai, Lu-Lu; Chen, Hai-Ting; Lai, Jing-Hui; Liu, Yao-Bin; Chen, Dong-Ping; Deng, Yu-Chun; Lin, Pan; Lin, Hua-Song; Hong, Bing-Cong; Yao, Qing-Yang; Chen, Xue-Jiao; Huang, Dan-Qin; Fu, Hong-Xia; Peng, Ji-Dong; Niu, Yan-Fang; Zhao, Yu-Ying; Zhu, Xiao-Qun; Lu, Xiao-Pei; Lin, Hai-Liang; Li, Yong-Kun; Liu, Chang-Yun; Huang, Gen-Bin; Wang, Ning; Chen, Wan-Jin.
Afiliação
  • Guo XX; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
  • Zou XH; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
  • Wang C; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
  • Yao XP; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
  • Su HZ; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
  • Lai LL; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
  • Chen HT; Department of Neurology, The Third Hospital of Xiamen, Xiamen, China.
  • Lai JH; Department of Neurology, Fujian University of Traditional Chinese Medicine Subsidiary Rehabilitation Hospital, Fuzhou, China.
  • Liu YB; Department of Neurology, Sanming Hospital of Integrated Traditional and Western Medicine, Sanming, China.
  • Chen DP; Department of Neurology, The Affiliated Longyan First Hospital of Fujian Medical University, Longyan, China.
  • Deng YC; Department of Neurology, Longyan People Hospital, Longyan, China.
  • Lin P; Department of Neurology, The Second Hospital of Longyan City, Longyan, China.
  • Lin HS; Department of Neurology, The Second Affiliated Hospital, Fujian Medical University, Quanzhou, China.
  • Hong BC; Department of Neurology, Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, China.
  • Yao QY; Department of Neurology, Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, China.
  • Chen XJ; Department of Neurology, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China.
  • Huang DQ; Department of Neurology, Wuyishan Municipal Hospital, Wuyishan, China.
  • Fu HX; Department of Neurology, Inner Mongolia People's Hospital, Hohhot, Inner Mongolia, China.
  • Peng JD; Department of Medical Imaging, Ganzhou People's Hospital, Ganzhou, China.
  • Niu YF; Department of Neurology, The Affiliated Hospital of Medical school, Ningbo University, Ningbo, China.
  • Zhao YY; Department of Neurology, Qilu Hospital of Shandong University, Jinan, China.
  • Zhu XQ; Department of Neurology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
  • Lu XP; Department of Neurology, The First Hospital of Fuzhou, Fuzhou, China.
  • Lin HL; Department of Neurology, Fuzhou Second Hospital, Fuzhou, China.
  • Li YK; Department of Neurology, Fujian Provincial Hospital, Provincial Clinical Department of Fujian Medical University, Fuzhou, China.
  • Liu CY; Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
  • Huang GB; Department of Internal Neurology, Ningde Municipal Hospital, Fujian Medical University, Ningde, China.
  • Wang N; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
  • Chen WJ; Fujian Key Laboratory of Molecular Neurology, Fuzhou, China.
Hum Mutat ; 40(4): 392-403, 2019 04.
Article em En | MEDLINE | ID: mdl-30609140
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encefalopatias / Calcinose / Doenças Neurodegenerativas / Predisposição Genética para Doença / Mutação País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encefalopatias / Calcinose / Doenças Neurodegenerativas / Predisposição Genética para Doença / Mutação País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China