Is 8860 variation a rare polymorphism or associated as a secondary effect in HCM disease?

INTRODUCTION: mtDNA defects, both deletions and point mutations, have been associated with hypertrophic cardiomyopathies. The aim of this study was to establish a spectrum for mtDNA mutations in Iranian hypertrophic cardiomyopathy (HCM) patients. MATERIAL AND METHODS: The control group was chosen am...

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Detalles Bibliográficos
Autores principales: Houshmand, Massoud, Montazeri, Maryam, Kuchekian, Nafiseh, Noohi, Freidoon, Nozar, Givtaj, Zamani, Akram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2011
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258716/
https://www.ncbi.nlm.nih.gov/pubmed/22291763
http://dx.doi.org/10.5114/aoms.2011.22074

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258716/
https://www.ncbi.nlm.nih.gov/pubmed/22291763
http://dx.doi.org/10.5114/aoms.2011.22074

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