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2-Methylbutyryl-coenzyme A dehydrogenase deficiency: a new inborn error of L-isoleucine metabolism.
Gibson, K M; Burlingame, T G; Hogema, B; Jakobs, C; Schutgens, R B; Millington, D; Roe, C R; Roe, D S; Sweetman, L; Steiner, R D; Linck, L; Pohowalla, P; Sacks, M; Kiss, D; Rinaldo, P; Vockley, J.
Affiliation
  • Gibson KM; Department of Molecular and Medical Genetics, Oregon Health Sciences University, Portland 97201, USA.
Pediatr Res ; 47(6): 830-3, 2000 Jun.
Article in En | MEDLINE | ID: mdl-10832746
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Oxidoreductases / Oxidoreductases Acting on CH-CH Group Donors / Amino Acid Metabolism, Inborn Errors / Isoleucine Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Infant / Male / Pregnancy Language: En Journal: Pediatr Res Year: 2000 Document type: Article Affiliation country:
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Oxidoreductases / Oxidoreductases Acting on CH-CH Group Donors / Amino Acid Metabolism, Inborn Errors / Isoleucine Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Infant / Male / Pregnancy Language: En Journal: Pediatr Res Year: 2000 Document type: Article Affiliation country: