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Pyruvate carboxylase deficiency. Report of a case and additional evidence for the "mild" phenotype.
Arnold, G L; Griebel, M L; Porterfield, M; Brewster, M.
Affiliation
  • Arnold GL; Department of Pediatrics, University of Rochester, School of Medicine and Dentistry, New York 14642, USA.
Clin Pediatr (Phila) ; 40(9): 519-21, 2001 Sep.
Article in En | MEDLINE | ID: mdl-11583052
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Pyruvate Carboxylase Deficiency Disease Type of study: Etiology_studies Limits: Child, preschool / Humans / Male Language: En Journal: Clin Pediatr (Phila) Year: 2001 Document type: Article Affiliation country: United States Country of publication: United States
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Pyruvate Carboxylase Deficiency Disease Type of study: Etiology_studies Limits: Child, preschool / Humans / Male Language: En Journal: Clin Pediatr (Phila) Year: 2001 Document type: Article Affiliation country: United States Country of publication: United States