Search
X-linked severe combined immunodeficiency (Swiss type agammaglobulinemia)
Genetics: - associated with defects in IL2RG Clinical manifestations: - less severe forms may be seen on the same genetic backgroundDatabase Correlations
OMIM correlations MORBIDMAP 308380References
- Noguchi et al. Cell 73:147-57 1993
- X-linked severe combined immunodeficiency http://ghr.nlm.nih.gov/condition=xlinkedseverecombinedimmunodeficiency