Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses-Reference-Cited by-同舟云学术

Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses

Published:2016-03 Issue: Volume:27 Page:32-38
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Vanlander Arnaud V.,Muiño Mosquera Laura,Panzer Joseph,Deconinck Tine,Smet Joél,Seneca Sara,Van Dorpe Jo,Ferdinande Liesbeth,Ceuterick-de Groote Chantal,De Jonghe Peter,Van Coster Rudy,Baets Jonathan

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference21 articles.

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2. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes;Barth;J Neurol Sci.,1983

3. Novel CHKB mutation expands the megaconial muscular dystrophy phenotype;Cabrera-Serrano;Muscle Nerve,2015

4. Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion;Castro-Gago;Eur. J. Paediatr. Neurol.,2014

5. Congenital megaconial myopathy due to a novel defect in the choline kinase Beta gene;Gutiérrez Ríos;Arch. Neurol.,2012

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