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[Clinical, biochemical and gene mutation characteristics of short chain acyl-coenzyme A dehydrogenase deficiency by neonatal screening].
Huang, X W; Zhang, Y; Yang, J B; Hong, F; Qian, G L; Tong, F; Mao, H Q; Huang, X L; Zhou, X L; Yang, R L; Zhao, Z Y.
Affiliation
  • Huang XW; Department of Genetics and Metabolism, Children's Hospital, Zhejiang University School of Medicine, Hangzhou 310052, China.
Zhonghua Er Ke Za Zhi ; 54(12): 927-930, 2016 Dec 02.
Article in Zh | MEDLINE | ID: mdl-27938594
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Full text: 1 Database: MEDLINE Main subject: Neonatal Screening / Acyl-CoA Dehydrogenase / Amino Acid Metabolism, Inborn Errors / Lipid Metabolism, Inborn Errors Type of study: Diagnostic_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Country/Region as subject: Asia Language: Zh Journal: Zhonghua Er Ke Za Zhi Year: 2016 Type: Article Affiliation country: China
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Full text: 1 Database: MEDLINE Main subject: Neonatal Screening / Acyl-CoA Dehydrogenase / Amino Acid Metabolism, Inborn Errors / Lipid Metabolism, Inborn Errors Type of study: Diagnostic_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Country/Region as subject: Asia Language: Zh Journal: Zhonghua Er Ke Za Zhi Year: 2016 Type: Article Affiliation country: China