Another step towards defining the genetic landscape of rhabdomyolysis-Reference-Cited by-同舟云学术

Another step towards defining the genetic landscape of rhabdomyolysis

Published:2021-09-01 Issue:9 Volume:144 Page:2560-2561
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

Author:

Ravenscroft Gianina¹²³^ORCID,Cabrera-Serrano Macarena⁴⁵^ORCID

Affiliation:

1. Harry Perkins Institute of Medical Research, Nedlands, WA, Australia

2. Centre for Medical Research, University of Western Australia, Nedlands, WA, Australia

3. School of Biomedical Sciences, University of Western Australia, Nedlands, WA, Australia

4. Unidad Enfermedades Neuromusculares, Servicio de Neurología y Neurofisiología Clínica, Hospital Universitario Virgen del Rocío, Sevilla, Spain

5. Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Sevilla, Spain

Abstract

This scientific commentary refers to ‘MLIP causes recessive myopathy with rhabdomyolysis, myalgia and baseline high serum creatine kinase’, by Lopes Abath Neto et al. (doi:10.1093/brain/awab275).

Funder

NHMRC

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awab308/40461389/awab308.pdf

Reference10 articles.

1. MLIP causes recessive myopathy with rhabdomyolysis, myalgia and baseline high serum creatine kinase;Lopes Abath Neto;Brain,2021

2. Muscle glycogenoses;DiMauro;Muscle Nerve,2001

3. CAV3 mutations causing exercise intolerance, myalgia and rhabdomyolysis: Expanding the phenotypic spectrum of caveolinopathies;Scalco;Neuromuscul Disord,2016

4. Expanding the phenotype of GMPPB mutations;Cabrera-Serrano;Brain,2015

5. Malignant hyperthermia associated with exercise-induced rhabdomyolysis or congenital abnormalities and a novel RYR1 mutation in New Zealand and Australian pedigrees;Davis;Br J Anaesth,2002

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Biallelic truncating variants in PACSIN3 cause childhood-onset myopathy with hyperCKaemia;Brain;2024-04-18

2. Cytokine release syndrome complicated with rhabdomyolysis after chimeric antigen receptor T-cell therapy: A case report;World Journal of Clinical Cases;2022-09-16