المؤلفون: Tang S; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., You J; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Liu L; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Ouyang H; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Jiang N; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Duan J; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Li C; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Luo Y; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Zhang W; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Zhan M; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Liu C; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China., Lyu GZ; AmCare Genomics Lab, Guangzhou, Guangdong, China., Zhang VW; AmCare Genomics Lab, Guangzhou, Guangdong, China., Zhao H; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.

المصدر: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Aug; Vol. 11 (8), pp. e2188. Date of Electronic Publication: 2023 Jul 24.

نوع المنشور: Case Reports; Journal Article; Review; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2324-9269 (Electronic) Linking ISSN: 23249269 NLM ISO Abbreviation: Mol Genet Genomic Med Subsets: MEDLINE

مواضيع طبية MeSH: Developmental Disabilities*/genetics , Developmental Disabilities*/pathology , Eye Diseases* , Intellectual Disability*/genetics , Intellectual Disability*/pathology , Malnutrition*, Child ; Female ; Humans ; Infant ; East Asian People ; Mutation ; Syndrome