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

Archives of Medical Science

Volumn 7, Issue 2, 2011, Pages 242-246

  Houshmand, Massoud ^a   Montazeri, Maryam ^a   Kuchekian, Nafiseh ^b   Noohi, Freidoon ^c   Nozar, Givtaj ^c   Zamani, Akram ^b  

^a NATIONAL INSTITUTE OF GENETIC ENGINEERING AND BIOTECHNOLOGY   (Iran)

^b Special Medical Center Iran   (Iran)

^c IRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Hypertrophic cardiomyopathy; mtDNA mutation disease

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; ENERGY METABOLISM; GENE DELETION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HEART CONTRACTION; HOSPITAL; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; IRAN; LINKAGE ANALYSIS; MITOCHONDRION; POINT MUTATION; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS;

EID: 79956346332     PISSN: 17341922     EISSN: None     Source Type: Journal    
DOI: 10.5114/aoms.2011.22074     Document Type: Article

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