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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Détails bibliographiques
Publié dans:PLoS One
Auteurs principaux: Jørgenrud, Benedicte, Jalanko, Mikko, Heliö, Tiina, Jääskeläinen, Pertti, Laine, Mika, Hilvo, Mika, Nieminen, Markku S., Laakso, Markku, Hyötyläinen, Tuulia, Orešič, Matej, Kuusisto, Johanna
Format: Artigo
Langue:Inglês
Publié: Public Library of Science 2015
Sujets:
Research Article
Accès en ligne: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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