The phenotypic and genotypic features of a Scottish cohort with McArdle disease-Reference-Cited by-同舟云学术

The phenotypic and genotypic features of a Scottish cohort with McArdle disease

Published:2021-08 Issue:8 Volume:31 Page:695-700
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Gandhi Sacha E.,Longman Cheryl,Petty Richard K.H.,Brennan Kathryn M.,Stewart Willie,Kinch Kevin,Töpf Ana,Straub Volker,Quinlivan Rosaline,Farrugia Maria Elena

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference32 articles.

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3. McArdle disease: a clinical review;Quinlivan;J Neurol Neurosurg Psychiatry,2010

4. Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry;Lucia;J Neurol Neurosurg Psychiatry,2012

5. Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update;Santalla;BMC Genom,2017

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5. Diagnosis and management of children with McArdle Syndrome (GSD V) in New South Wales;JIMD Reports;2023-08-09