Your browser doesn't support javascript.
loading
A novel PMP22 insertion mutation causing Charcot-Marie-Tooth disease type 3: A case report.
Han, Liang; Huang, Yanjing; Nie, Yuan; Li, Jing; Chen, Gang; Tu, Shenghao; Shen, Pan; Chen, Chao.
Afiliação
  • Han L; Department of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan.
  • Huang Y; Department of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan.
  • Nie Y; Rehabilitation Center, Qijiang District Hospital of Traditional Chinese Medicine, 50 Dashi Road of Wenlong Avenue, Chongqing.
  • Li J; Department of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan.
  • Chen G; Department of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan.
  • Tu S; Department of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan.
  • Shen P; Department of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan.
  • Chen C; Department of Orthopaedics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Avenue, Wuhan, China.
Medicine (Baltimore) ; 100(11): e25163, 2021 Mar 19.
Article em En | MEDLINE | ID: mdl-33726003
Assuntos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuropatia Hereditária Motora e Sensorial / Mutagênese Insercional / Proteínas da Mielina Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2021 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuropatia Hereditária Motora e Sensorial / Mutagênese Insercional / Proteínas da Mielina Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2021 Tipo de documento: Article País de publicação: Estados Unidos