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Is l-Carnitine Supplementation Beneficial in 3-Methylcrotonyl-CoA Carboxylase Deficiency?

Background: 3-Methylcrotonyl-CoA carboxylase deficiency (3-MCCd) is an autosomal recessive disorder in the catabolism of leucine. In the present study, we investigated the current and prior medical condition of patients with 3-MCCd in the Faroe Islands and their carnitine levels in blood, urine and...

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Publicado en:JIMD Rep
Main Authors: Thomsen, Jákup Andreas, Lund, Allan Meldgaard, Olesen, Jess Have, Mohr, Magni, Rasmussen, Jan
Formato: Artigo
Idioma:Inglês
Publicado: Springer Berlin Heidelberg 2015
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4470948/
https://ncbi.nlm.nih.gov/pubmed/25732994
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2014_393
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