Hypothyroidism in late-onset Pompe disease

PURPOSE: In Pompe disease, a deficiency of acid α-glucosidase enzyme activity leads to pathologic accumulation of glycogen in tissues. Phenotype heterogeneity in Pompe includes an infantile form and late-onset forms (juvenile- and adult-onset forms). Symptoms common to all phenotypes include progres...

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Detalles Bibliográficos
Publicado en:Mol Genet Metab Rep
Autores principales: Schneider, Joseph, Burmeister, Lynn A., Rudser, Kyle, Whitley, Chester B., Jarnes Utz, Jeanine
Formato: Artigo
Lenguaje:Inglês
Publicado: Elsevier 2016
Materias:
Research Paper
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4932620/
https://ncbi.nlm.nih.gov/pubmed/27408821
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgmr.2016.06.002
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