AMPD1 gene mutations are associated with obesity and diabetes in Polish patients with cardiovascular diseases

Previous studies showed an association of the common functional polymorphism (C34T, Gln12Stop) in the adenosine monophosphate deaminase-1 (AMPD1) gene with survival in heart failure (HF) and/or coronary artery disease (CAD). The aim of the study was to search for other mutations in selected regions...

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Detalhes bibliográficos
Main Authors: Safranow, Krzysztof, Suchy, Janina, Jakubowska, Katarzyna, Olszewska, Maria, Bińczak-Kuleta, Agnieszka, Kurzawski, Grzegorz, Rzeuski, Ryszard, Czyżycka, Edyta, Łoniewska, Beata, Kornacewicz-Jach, Zdzisława, Ciechanowicz, Andrzej, Chlubek, Dariusz
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2010
Assuntos:
Human genetics · Short Communication
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3026686/
https://ncbi.nlm.nih.gov/pubmed/21108053
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13353-010-0009-x
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