ISSN 2149-2263 | E-ISSN 2149-2271
pdf
Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation [Anatol J Cardiol]
Anatol J Cardiol. 2018; 20(1): 65-68 | DOI: 10.14744/AnatolJCardiol.2018.69639

Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation

Najlae Adadi1, Fatima Zohra Radi3, Najim Lahrouchi4, Loubna Hara3, Ilham Ratbi1, Siham Chafai Elalaoui1, Marielle Alders5, Jamila Zarzur3, Connie Bezzina4, Abdelaziz Sefiani2
1Research Center in Genomics of Human Pathologies (GENOPATH), Faculty of Medicine and Pharmacy, Mohammed V University in Rabat; Rabat-Morocco
2Department of Cardiology B, Mohammed V University, Souissi; Rabat-Morocco
3Department of Experimental Cardiology, Heart Center, Amsterdam Medical Center, University of Amsterdam; Amsterdam-The Netherlands
4Department of Clinical Genetics, Academic Medical Center, University of Amsterdam; Amsterdam-The Netherlands
5Department of Medical Genetics, National Institute of Health; Rabat-Morocco

Keywords: Cardiomyopathies, Dilated Cardiomyopathy, LMNA gene, mutation, Moroccan family.

Najlae Adadi, Fatima Zohra Radi, Najim Lahrouchi, Loubna Hara, Ilham Ratbi, Siham Chafai Elalaoui, Marielle Alders, Jamila Zarzur, Connie Bezzina, Abdelaziz Sefiani. Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation. Anatol J Cardiol. 2018; 20(1): 65-68

Corresponding Author: Najlae Adadi, Morocco
Manuscript Language: English


Journal Metrics

Journal Citation Indicator: 0.18
CiteScore: 1.1
Source Normalized Impact
per Paper:
0.22
SCImago Journal Rank: 0.348

Quick Search



Copyright © 2024 The Anatolian Journal of Cardiology



Kare Publishing is a subsidiary of Kare Media.