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Indentification of novel MSTO1 compound heterozygous mutations in a Chinese family with recessive cerebellar atrophy and ataxia.
Chen, Jia; Xiao, Junfang; Chen, Ge; Xu, Qiang; Wu, Xingwu; Tian, Lifeng; Huang, Zhihui; Xin, Cailin; Zhao, Yan; Guo, Zhen; Zou, Yang; Wu, Qiongfang.
Afiliação
  • Chen J; Reproductive Medicine Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, China.
  • Xiao J; Medical Genetics Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, China.
  • Chen G; Jiangxi Provincial Key Laboratory of Birth Defect for Prevention and Control, Nanchang, China.
  • Xu Q; Central Laboratory, Jiangxi Provincial Maxternal and Child Health Hospital, Nanchang, China.
  • Wu X; Reproductive Medicine Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, China.
  • Tian L; Reproductive Medicine Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, China.
  • Huang Z; Reproductive Medicine Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, China.
  • Xin C; Reproductive Medicine Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, China.
  • Zhao Y; Reproductive Medicine Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, China.
  • Guo Z; Reproductive Medicine Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, China.
  • Zou Y; Medical Imaging Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, China.
  • Wu Q; Central Laboratory, Jiangxi Provincial Maxternal and Child Health Hospital, Nanchang, China.
Front Neurol ; 13: 988519, 2022.
Article em En | MEDLINE | ID: mdl-36468072
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Front Neurol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Front Neurol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China