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The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathy
BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a primary disorder characterised by asymmetric thickening of septum and left ventricular wall, with a prevalence of 0.2% in the general population. OBJECTIVE: To describe a novel mitochondrial DNA mutation and its association with the pathogenesis of...
Gorde:
| Egile Nagusiak: | , , , , , , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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BMJ Publishing Group
2014
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3932983/ https://ncbi.nlm.nih.gov/pubmed/24367055 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2013-101818 |
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