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...

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Detalles Bibliográficos
Autores principales: Liu, Zhong, Song, Yanrui, Li, Dan, He, Xiangyu, Li, Shishi, Wu, Bifeng, Wang, Wei, Gu, Shulian, Zhu, Xiaoyu, Wang, Xuexiang, Zhou, Qiyin, Dai, Yu, Yan, Qingfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Genotype-Phenotype Correlations
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932983/
https://www.ncbi.nlm.nih.gov/pubmed/24367055
http://dx.doi.org/10.1136/jmedgenet-2013-101818

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932983/
https://www.ncbi.nlm.nih.gov/pubmed/24367055
http://dx.doi.org/10.1136/jmedgenet-2013-101818

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