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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Detalles Bibliográficos
Autores principales: Jørgenrud, Benedicte, Jalanko, Mikko, Heliö, Tiina, Jääskeläinen, Pertti, Laine, Mika, Hilvo, Mika, Nieminen, Markku S., Laakso, Markku, Hyötyläinen, Tuulia, Orešič, Matej, Kuusisto, Johanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534205/
https://www.ncbi.nlm.nih.gov/pubmed/26267065
http://dx.doi.org/10.1371/journal.pone.0134184

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534205/
https://www.ncbi.nlm.nih.gov/pubmed/26267065
http://dx.doi.org/10.1371/journal.pone.0134184

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