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Case Report: Congenital Myasthenic Syndrome Presenting with Bilateral Vocal Cord Paralysis Caused by De-Novel Compound Heterozygous MUSK Mutation.
Jiang, Lan; Wang, Sheng-Cai; Zhang, Jie; Han, Fu-Gen; Zhao, Jing; Xu, Ying.
Afiliação
  • Jiang L; Department of Otorhinolaryngology Head and Neck Surgery, Children's Hospital Affiliated to Zhengzhou University; Henan Children's Hospital; Zhengzhou Children's Hospital, Zhengzhou, 450003, People's Republic of China.
  • Wang SC; National Center for Children's Health, Department of Otolaryngology Head and Neck Surgery, Beijing Children's Hospital, Capital Medical University, Beijing, 100045, People's Republic of China.
  • Zhang J; National Center for Children's Health, Department of Otolaryngology Head and Neck Surgery, Beijing Children's Hospital, Capital Medical University, Beijing, 100045, People's Republic of China.
  • Han FG; Department of Otorhinolaryngology Head and Neck Surgery, Children's Hospital Affiliated to Zhengzhou University; Henan Children's Hospital; Zhengzhou Children's Hospital, Zhengzhou, 450003, People's Republic of China.
  • Zhao J; National Center for Children's Health, Department of Otolaryngology Head and Neck Surgery, Beijing Children's Hospital, Capital Medical University, Beijing, 100045, People's Republic of China.
  • Xu Y; Department of Otorhinolaryngology Head and Neck Surgery, Children's Hospital Affiliated to Zhengzhou University; Henan Children's Hospital; Zhengzhou Children's Hospital, Zhengzhou, 450003, People's Republic of China.
Pharmgenomics Pers Med ; 16: 373-379, 2023.
Article em En | MEDLINE | ID: mdl-37091828
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article