منابع مشابه
The molecular genetics of arrhythmias.
It was only ten years ago that mutations in ion channel genes were first described in patients with the long QT syndrome (LQTS) [1]. Since then, mutations in a total of eight different sarcolemmal ion channel subunit genes (KCNQ1, KCNH2, KCNE1, KCNE2, SCN5A, KCNJ2, HCN4, CACNA1C), two genes encoding sarcoplasmic reticulum (SR) Ca handling proteins (RYR2, CASQ2), and an anchoring protein gene (A...
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genetic basis of diffrent arrhythmias has always been an intresting subject of resesrch for scientists. here i will review in brief the most common familia arrhythmias and the new findings regarding their mode of inhetitance. this paper will mainly focus on the genetic basis of the long qt syndromes but we will also have a short review of the genetics of three other familia congenital arrhythmo...
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متن کاملGenetics of cardiac arrhythmias.
Correspondence to: Dr Arthur A M Wilde, Experimental & Molecular Cardiology Group, Academic Medical Center, Amsterdam, the Netherlands; a.a.wilde@ amc.uva.nl _________________________ O ver the last decade, we have witnessed a revolution in the understanding of primary cardiac arrhythmia syndromes. These remarkable advances stemmed from the discovery of mutations, primarily in ion channel genes...
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Background: Vitiligo is an acquired, idiopathic, and common depigmentation disorder of the skin that affects people of all ages and both sexes equally in the worldwide. Although etiology of the disease is unknown, there are theories such as environment and genetic factors. Methods: In this article, we collected and summarized the appropriate manuscripts regarding the epidemiology and gene...
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ژورنال
عنوان ژورنال: Cardiovascular Research
سال: 2005
ISSN: 0008-6363
DOI: 10.1016/j.cardiores.2005.06.004