Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease.

Ravell, Juan C

Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease. [electronic resource] - The Journal of clinical investigation 01 2020 - 507-522 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't

1558-8238

10.1172/JCI131116 doi


Antigens, CD--genetics
Autoimmune Lymphoproliferative Syndrome--genetics
CD4-CD8 Ratio
Cation Transport Proteins--genetics
Female
Glycosylation
Humans
Magnesium Deficiency--genetics
Male
X-Linked Combined Immunodeficiency Diseases--genetics