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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...
Autores principales: | Houshmand, Massoud, Montazeri, Maryam, Kuchekian, Nafiseh, Noohi, Freidoon, Nozar, Givtaj, Zamani, Akram |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2011
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Materias: | |
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 |
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