Novel mitochondrial DNA mutations in a rare variety of hypertrophic cardiomyopathy

被引：20

作者：

Prasad, GN

Vanniarajan, A

Emmanuel, C

Cherian, KM

Singh, L

Thangaraj, K

机构：

[1] Int Ctr Cardio Thorac & Vasc Dis, A Unit Fontier Lifeline, KM Cherian Heart Fdn, Madras 600101, Tamil Nadu, India

[2] Ctr Cellular & Mol Biol, Hyderabad 500007, Andhra Pradesh, India

来源：

INTERNATIONAL JOURNAL OF CARDIOLOGY | 2006年 / 109卷 / 03期

关键词：

hypertrophic cardiomyopathy; midcavity obstruction; arrhythmias; mitochondria; mitochondrial DNA mutation;

D O I：

10.1016/j.ijcard.2005.07.065

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

We report a rare case of a 65 year old male with mid left ventricular cavity obstruction which is an uncommon form of hypertrophic cardionryopathy with cytogenetic analysis revealing novel mutations in mitochondrial nucleic acid. (c) 2005 Elsevier Ireland Ltd. All rights reserved.

引用

页码：432 / 433

页数：2

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