A Novel LAS1L Gene Mutation Associated with Impaired Growth and Developmental Delay and a Review with Previously Reported Cases.

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Title: A Novel LAS1L Gene Mutation Associated with Impaired Growth and Developmental Delay and a Review with Previously Reported Cases.
Authors: Mostafavi N; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.; Hubei Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Wuhan 430030, China.; Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Wuhan 430030, China.; State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Wuhan 430030, China., Tian A; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.; Hubei Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Wuhan 430030, China.; Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Wuhan 430030, China.; State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Wuhan 430030, China., Gao Y; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.; Hubei Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Wuhan 430030, China.; Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Wuhan 430030, China.; State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Wuhan 430030, China., Li Y; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.; Hubei Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Wuhan 430030, China.; Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Wuhan 430030, China.; State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Wuhan 430030, China., Liang F; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.; Hubei Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Wuhan 430030, China.; Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Wuhan 430030, China.; State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Wuhan 430030, China., Zhang C; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.; Hubei Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Wuhan 430030, China.; Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Wuhan 430030, China.; State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Wuhan 430030, China., Luo X; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.; Hubei Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Wuhan 430030, China.; Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Wuhan 430030, China.; State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Wuhan 430030, China.
Source: Genes [Genes (Basel)] 2026 Jun 20; Vol. 17 (6). Date of Electronic Publication: 2026 Jun 20.
Publication Type: Journal Article; Case Reports; Review; Research Support, Non-U.S. Gov't
Journal Info: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:2073-4425
DOI:10.3390/genes17060708