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Novel frameshift mutation in the AHDC1 gene in a Chinese global developmental delay patient: A case report.
Lin, Shuang-Zhu; Xie, Hong-Yan; Qu, Yan-Lai; Gao, Wen; Wang, Wan-Qi; Li, Jia-Yi; Feng, Xiao-Chun; Jin, Chun-Quan.
Afiliação
  • Lin SZ; Diagnosis and Treatment Center for Children, The First Affiliated Hospital to Changchun University of Chinese Medicine, Changchun 130021, Jilin Province, China.
  • Xie HY; Diagnosis and Treatment Center for Children, The First Affiliated Hospital to Changchun University of Chinese Medicine, Changchun 130021, Jilin Province, China.
  • Qu YL; Diagnosis and Treatment Center for Children, The First Affiliated Hospital to Changchun University of Chinese Medicine, Changchun 130021, Jilin Province, China.
  • Gao W; Changchun University of Chinese Medicine, Changchun 130000, Jilin Province, China.
  • Wang WQ; Changchun University of Chinese Medicine, Changchun 130000, Jilin Province, China.
  • Li JY; Changchun University of Chinese Medicine, Changchun 130000, Jilin Province, China.
  • Feng XC; Diagnosis and Treatment Center for Children, The First Affiliated Hospital to Changchun University of Chinese Medicine, Changchun 130021, Jilin Province, China.
  • Jin CQ; Diagnosis and Treatment Center for Children, The First Affiliated Hospital to Changchun University of Chinese Medicine, Changchun 130021, Jilin Province, China. jinchunquan@126.com.
World J Clin Cases ; 10(21): 7517-7522, 2022 Jul 26.
Article em En | MEDLINE | ID: mdl-36157999

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: World J Clin Cases Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: World J Clin Cases Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China