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An X-linked PLXNB3 mutation identified in patients with congenital heart disease with neurodevelopmental disabilities.
Feng, Zhiyu; Chen, Xinyuan; Li, Ting; Gao, Han; Chen, Weicheng; Gao, Yuan; Yao, Qinyu; Zhuang, Quannan; Ma, Xiaojing; Sheng, Wei; Xie, Yuquan; Huang, Guoying.
Affiliation
  • Feng Z; Institutes of Biomedical Sciences, and Children's Hospital of Fudan University, Shanghai, China.
  • Chen X; Shanghai Key Laboratory of Birth Defects, Shanghai, China.
  • Li T; State Key Laboratory for Oncogenes and Related Genes, Division of Cardiology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Cancer Institute, Shanghai, China.
  • Gao H; Shanghai Key Laboratory of Birth Defects, Shanghai, China.
  • Chen W; Shanghai Key Laboratory of Birth Defects, Shanghai, China.
  • Gao Y; Shanghai Key Laboratory of Birth Defects, Shanghai, China.
  • Yao Q; Shanghai Key Laboratory of Birth Defects, Shanghai, China.
  • Zhuang Q; Shanghai Key Laboratory of Birth Defects, Shanghai, China.
  • Ma X; Shanghai Key Laboratory of Birth Defects, Shanghai, China.
  • Sheng W; Shanghai Key Laboratory of Birth Defects, Shanghai, China.
  • Xie Y; Institutes of Biomedical Sciences, and Children's Hospital of Fudan University, Shanghai, China.
  • Huang G; Shanghai Key Laboratory of Birth Defects, Shanghai, China.
Transl Pediatr ; 11(11): 1852-1863, 2022 Nov.
Article in En | MEDLINE | ID: mdl-36506778
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Transl Pediatr Year: 2022 Document type: Article Affiliation country: China Country of publication: China
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Transl Pediatr Year: 2022 Document type: Article Affiliation country: China Country of publication: China