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PCDH19-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency.
Chen, Yi; Yang, Xiaoxu; Chen, Jiaoyang; Yang, Xiaoling; Yang, Ying; Liu, Aijie; Zhang, Xiaoli; Wu, Wenjuan; Sun, Dan; Yang, Zhixian; Jiang, Yuwu; Zhang, Yuehua.
Affiliation
  • Chen Y; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Yang X; Center for Bioinformatics, State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Peking University, Beijing, China.
  • Chen J; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Yang X; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Yang Y; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Liu A; Department of Pediatric Neurology, Capital Institute of Pediatrics, Beijing, China.
  • Zhang X; Department of Pediatrics, The Third Affiliated Hospital of Zheng Zhou University, Zhengzhou, China.
  • Wu W; Department of Neurology, Hebei Children's Hospital, Shijiazhuang, China.
  • Sun D; Department of Neurology, Wuhan Children's Hospital, Wuhan, China.
  • Yang Z; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Jiang Y; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Zhang Y; Department of Pediatrics, Peking University First Hospital, Beijing, China.
Front Neurol ; 13: 1041509, 2022.
Article in En | MEDLINE | ID: mdl-36408521
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Front Neurol Year: 2022 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Front Neurol Year: 2022 Document type: Article Affiliation country: Country of publication: