The Metabolome in Finnish Carriers of the MYBPC3-Q1061X Mutation for Hypertrophic Cardiomyopathy

AIMS: Mutations in the cardiac myosin-binding protein C gene (MYBPC3) are the most common genetic cause of hypertrophic cardiomyopathy (HCM) worldwide. The molecular mechanisms leading to HCM are poorly understood. We investigated the metabolic profiles of mutation carriers with the HCM-causing MYBP...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Jørgenrud, Benedicte, Jalanko, Mikko, Heliö, Tiina, Jääskeläinen, Pertti, Laine, Mika, Hilvo, Mika, Nieminen, Markku S., Laakso, Markku, Hyötyläinen, Tuulia, Orešič, Matej, Kuusisto, Johanna
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2015
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4534205/
https://ncbi.nlm.nih.gov/pubmed/26267065
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0134184
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