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PYGM mRNA expression in McArdle disease: Demographic, clinical, morphological and genetic features

INTRODUCTION: McArdle disease presents clinical and genetic heterogeneity. There is no obvious association between genotype and phenotype. PYGM (muscle glycogen phosphorylase gene) mRNA expression and its association with clinical, morphological, and genetic aspects of the disease as a set have not...

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Detalles Bibliográficos
Autores principales: Carvalho, Alzira A. S., Christofolini, Denise M., Perez, Matheus M., Alves, Beatriz C. A., Rodart, Itatiana, Figueiredo, Francisco W. S., Turke, Karine C., Feder, David, Junior, Marcondes C. F., Nucci, Ana M., Fonseca, Fernando L. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394413/
https://www.ncbi.nlm.nih.gov/pubmed/32735634
http://dx.doi.org/10.1371/journal.pone.0236597