Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathy-Reference-Cited by-同舟云学术

Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathy

Published:2017-05-18 Issue:6 Volume:92 Page:616-623
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Janin A.¹²,N'Guyen K.³,Habib G.⁴,Dauphin C.⁵,Chanavat V.¹²,Bouvagnet P.²⁶,Eschalier R.⁵,Streichenberger N.²⁷,Chevalier P.⁸,Millat G.¹²^ORCID

Affiliation:

1. Laboratoire de Cardiogénétique Moléculaire; Centre de Biologie et Pathologie Est, Hospices Civils de Lyon; Lyon France

2. NeuroMyoGen Institute, CNRS UMR 5310 - INSERM U1217, Université de Lyon 1; Lyon France

3. Department of Medical Genetics; Timone Hospital, Marseille Teaching Hospital; Marseille France

4. Cardiology Department; Timone Hospital; Marseille France

5. Image Science for Interventional Techniques (ISIT), UMR6284, and CHU Clermont-Ferrand, Cardiology Department; Clermont Université, Université d'Auvergne, Cardio Vascular Interventional Therapy and Imaging (CaVITI); Clermont-Ferrand France

6. Groupe Hospitalier Est, Hospices Civils de Lyon; Service de Cardiologie C; Lyon France

7. Laboratoire d'Anatomo-Cyto-Pathologie, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon; Lyon France

8. Hôpital Cardiologique Louis-Pradel; Service de Rythmologie; Bron France

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13043/fullpdf

Reference25 articles.

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2. Heart disease and stroke statistics 2015 update: a report from the American Heart Association;Mozaffarian;Circulation,2015

3. Atlas of the clinical genetics of human dilated cardiomyopathy;Haas;Eur Heart J,2015

4. The rationale and timing of molecular genetic testing for dilated cardiomyopathy;Morales;Can J Cardiol,2015

5. A fast and cost-effective molecular diagnostic tool for genetic diseases involved in sudden cardiac death;Chanavat;Clin Chim Acta,2016

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