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Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients.

We describe two patients with short-chain acyl-coenzyme A (CoA) dehydrogenase (SCADH) deficiency. Neonate I excreted large amounts of ethylmalonate and methylsuccinate; ethylmalonate excretion increased after a medium-chain triglyceride load. Neonate II died postnatally and excreted ethylmalonate, b...

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Detaylı Bibliyografya
Asıl Yazarlar: Amendt, B A, Greene, C, Sweetman, L, Cloherty, J, Shih, V, Moon, A, Teel, L, Rhead, W J
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1987
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC424368/
https://ncbi.nlm.nih.gov/pubmed/3571488
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