Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene in Hypertrophic Cardiomyopathy Patients

Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene in Hypertrophic Cardiomyopathy Patients

Abstract Background: Hypertrophic cardiomyopathy (HCM) is a various collection of heart diseases with autosomal dominant inheritance affecting 0.2% of the global population. HCM is also the most common cause of sudden cardiac death in individuals younger than 35 years old. Approximately, 40% of aff...

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Bibliographic Details
Main Authors: Behnaz Sadat Abedi, Seyedeh Zohreh kiyani, Morteza Hashemzadeh Chaleshtori, Shahrbanoo Parchami, Abbas Doosti
Format: Article
Language:fas
Published: Arak Medical University 2015-08-01
Series:Majallah-i dānishgāh-i ̒ulūm-i pizishkī-i Arāk
Subjects:
Heteroduplex analysis
Hypertrophic cardiomyopathy
Myosin-binding protein C3 Mutation
Single-stranded conformational polymorphism.
Online Access:http://amuj.arakmu.ac.ir/article-1-3441-en.pdf

Internet

http://amuj.arakmu.ac.ir/article-1-3441-en.pdf

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