Prevalence of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency in Estonia

The aim of our study was to evaluate the prevalence of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) in the general Estonian population and among patients with symptoms suggestive of fatty acid oxidation (FAO) defects. We collected DNA from a cohort of 1,040 anonymous newborn blood...

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Detaylı Bibliyografya
Asıl Yazarlar: Joost, K., Õunap, K., Žordania, R., Uudelepp, M.-L., Olsen, R. K., Kall, K., Kilk, K., Soomets, U., Kahre, T.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer Berlin Heidelberg 2011
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3509831/
https://ncbi.nlm.nih.gov/pubmed/23430857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2011_51
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