A patient with glycogen storage disease type 0 and a novel sequence variant in GYS2: a case report and literature review

Glycogen storage disease type 0 (GSD0) is an autosomal recessive disorder caused by a sequence variant in the GYS2 gene, leading to decreased or absent activity of hepatic glycogen synthase. With a frequency of less than 1 in 1,000,000 individuals, GSD0 represents only around 1% of all glycogen stor...

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Detalles Bibliográficos
Autores principales: Arko, Janez Jan, Debeljak, Marusa, Tansek, Mojca Zerjav, Battelino, Tadej, Groselj, Urh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425267/
https://www.ncbi.nlm.nih.gov/pubmed/32779500
http://dx.doi.org/10.1177/0300060520936857

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425267/
https://www.ncbi.nlm.nih.gov/pubmed/32779500
http://dx.doi.org/10.1177/0300060520936857

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