GAA variants associated with reduced enzymatic activity but lack of Pompe-related symptoms, incidentally identified by exome sequencing

Pompe disease is a rare metabolic myopathy caused by pathogenic variants affecting the activity of the lysosomal glycogen-degrading enzyme acid alpha-glucosidase (GAA). Impaired GAA function results in the accumulation of undegraded glycogen within lysosomes in multiple tissues but predominantly aff...

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Detalles Bibliográficos
Autores principales: Malekkou, Anna, Theodosiou, Athina, Alexandrou, Angelos, Papaevripidou, Ioannis, Sismani, Carolina, Jacobs, Edwin H., Ruijter, George J.G., Anastasiadou, Violetta, Ourani, Sofia, Athanasiou, Emilia, Drousiotou, Anthi, Grafakou, Olga, Petrou, Petros P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433214/
https://www.ncbi.nlm.nih.gov/pubmed/37600231
http://dx.doi.org/10.1016/j.ymgmr.2023.100997

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433214/
https://www.ncbi.nlm.nih.gov/pubmed/37600231
http://dx.doi.org/10.1016/j.ymgmr.2023.100997

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