Your browser doesn't support javascript.
loading
Clinical features and mutations in seven Chinese patients with very long chain acyl-CoA dehydrogenase deficiency.
Zhang, Rui-Nan; Li, Yi-Fan; Qiu, Wen-Juan; Ye, Jun; Han, Lian-Shu; Zhang, Hui-Wen; Lin, Na; Gu, Xue-Fan.
Affiliation
  • Zhang RN; Department of Pediatric Endocrinology and Genetic Metabolism and Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200092, China.
World J Pediatr ; 10(2): 119-25, 2014 May.
Article in En | MEDLINE | ID: mdl-24801231
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acyl-CoA Dehydrogenase, Long-Chain / Lipid Metabolism, Inborn Errors / Mutation Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Child / Female / Humans / Infant / Male / Newborn Country/Region as subject: Asia Language: En Journal: World J Pediatr Journal subject: PEDIATRIA Year: 2014 Document type: Article Affiliation country: China Country of publication: Suiza
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acyl-CoA Dehydrogenase, Long-Chain / Lipid Metabolism, Inborn Errors / Mutation Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Child / Female / Humans / Infant / Male / Newborn Country/Region as subject: Asia Language: En Journal: World J Pediatr Journal subject: PEDIATRIA Year: 2014 Document type: Article Affiliation country: China Country of publication: Suiza