First application of next-generation sequencing in patients with hypertrophic cardiomyopathy in Morocco and report of a novel frameshift mutation of MYBPC3 gene: Case report-Reference-Cited by-同舟云学术

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First application of next-generation sequencing in patients with hypertrophic cardiomyopathy in Morocco and report of a novel frameshift mutation of MYBPC3 gene: Case report

Published:2019-12 Issue: Volume:22 Page:100590
ISSN:2214-5400
Container-title:Meta Gene
language:en
Short-container-title:Meta Gene

Author:

Adadi Najlae^ORCID,Zrhidri Abdelali,Fellat Ibtissam,Bouzelmat Hicham,Benzaroual Dounia,Bouhouch Rachida,Radi Fatima Zohra,Lyahyai Jaber,Ratbi Ilham,Sefiani Abdelaziz

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference12 articles.

1. Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all;Callis;Expert. Rev. Mol. Diagn.,2010

2. Review of recent advances in the management of hypertrophic cardiomyopathy;Cao;Eur. Rev. Med. Pharmacol. Sci.,2017

3. Targeted next-generation sequencing (NGS) of nine candidate genes with custom AmpliSeq in patients and a cardiomyopathy risk group;Glotov;Clin. Chim. Acta,2015

4. A missense mutation of cardiac beta-myosin heavy chain gene linked to familial hypertrophic cardiomyopathy in affected Japanese families;Harada;Biochem. Biophys. Res. Commun.,1993

5. Isolated X-linked hypertrophic cardiomyopathy caused by a novel mutation of the four-and-a-half LIM domain 1 gene;Hartmannova;Circ. Cardiovasc. Genet.,2013

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