Immune dysregulation in Glycogen Storage Disease 1b - a CyTOF approach

Glycogen Storage Disease type 1b (GSD1b) is a rare disease manifesting as hypoglycemia, recurrent infections and neutropenia, resulting from deleterious mutations in the SLC37A4 gene encoding the glucose-6-phosphate transporter. The susceptibility to infections is thought to be attributed not only t...

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Detalles Bibliográficos
Autores principales: Gehlhaar, Arne, Shouval, Dror, Santiago, Eduardo Gonzalez, Ling, Galina, McCourt, Blake, Werner, Lael, Yerushalmi, Baruch, Konnikova, Liza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980199/
https://www.ncbi.nlm.nih.gov/pubmed/36865166
http://dx.doi.org/10.21203/rs.3.rs-2598829/v1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980199/
https://www.ncbi.nlm.nih.gov/pubmed/36865166
http://dx.doi.org/10.21203/rs.3.rs-2598829/v1

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