Associated Papers
McArdle Disease: New Insights into Its Underlying Molecular Mechanisms.
Llavero F et al.
International Journal of Molecular Sciences, 2019
Novel myophosphorylase mutation (p.Arg94Pro) with progressive exercise intolerance.
Nabavi Nouri M et al.
Clinical Case Reports, 2018
Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update.
Santalla A et al.
Bmc Genomics, 2017
Select a paper to view details