Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans-Reference-Cited by-同舟云学术

Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans

Published:2010-10 Issue:2-3 Volume:101 Page:178-182
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

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

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference35 articles.

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3. Neuropathological, biochemical and molecular findings in a glutaric acidemia type 1 cohort;Funk;Brain,2005

4. Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiency;Sauer;J. Inherit. Metab. Dis.,2007

5. Acylcarnitines, Including In Vitro Loading Tests;Matern,2008

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