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Glutaric aciduria type 1 in South Africa-high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans.
van der Watt, George; Owen, Elizabeth P; Berman, Peter; Meldau, Surita; Watermeyer, Nicholas; Olpin, Simon E; Manning, Nigel J; Baumgarten, Ingrid; Leisegang, Felicity; Henderson, Howard.
Affiliation
  • van der Watt G; Division of Chemical Pathology, Groote Schuur and Red Cross Children's Hospitals, University of Cape Town, Cape Town, South Africa. george.vanderwatt@uct.ac.za
Mol Genet Metab ; 101(2-3): 178-82, 2010.
Article in En | MEDLINE | ID: mdl-20732827
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glutaryl-CoA Dehydrogenase Type of study: Incidence_studies / Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: Africa Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2010 Document type: Article Affiliation country: South Africa Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glutaryl-CoA Dehydrogenase Type of study: Incidence_studies / Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: Africa Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2010 Document type: Article Affiliation country: South Africa Country of publication: United States