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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...
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. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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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 |
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