Development of Continuum of Care for McArdle disease: A practical tool for clinicians and patients

Author:

Reason S.L.ORCID,Voermans N.,Lucia A.,Vissing J.,Quinlivan R.,Bhai S.,Wakelin A.

Publisher

Elsevier BV

Subject

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

Reference30 articles.

1. Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database;Nguengang Wakap;Eur J Hum Genet,2020

2. The national economic burden of rare disease in the United States in 2019;Yang;Orphanet J Rare Dis,2022

3. Healthcare access, satisfaction, and health-related quality of life among children and adults with rare diseases;Bogart;Orphanet J Rare Dis,2022

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

5. McArdle disease: new insights into its underlying molecular mechanisms;Llavero;Int J Mol Sci,2019

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