Syndromic PRD: case report of McArdle retinopathy and review of literature-Reference-Cited by-同舟云学术

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Syndromic PRD: case report of McArdle retinopathy and review of literature

Published:2024-08 Issue:4 Volume:59 Page:e415-e419
ISSN:0008-4182
Container-title:Canadian Journal of Ophthalmology
language:en
Short-container-title:Canadian Journal of Ophthalmology

Author:

Abdul Rahman^ORCID,Fazio Timothy^ORCID,Savige Judy,Mack Heather G.^ORCID

Funder

Novartis

Publisher

Elsevier BV

Reference37 articles.

1. Proteomics: tissue-based map of the human proteome;Uhlén;Science,2015

2. FANTOM5 CAGE profiles of human and mouse reprocessed for GRCh38 and GRCm38 genome assemblies;Abugessaisa;Sci Data,2017

3. Myopathy due to a defect in muscle glycogen breakdown;McArdle;Clin Sci,1951

4. High-resolution chromosome sorting and DNA spot-blot analysis assign McArdle's syndrome to chromosome 11;Lebo;Science,1984

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

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