Analysis of mutations in the IL2RG gene in 2 asian infants with X-linked severe combined immunodeficiency
J. investig. allergol. clin. immunol
; 25(4): 313-315, 2015. ilus
Article
in English
| IBECS
| ID: ibc-138435
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
No disponible
Full text:
Available
Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
X-Linked Combined Immunodeficiency Diseases
/
Interleukin Receptor Common gamma Subunit
/
Hypersensitivity
Limits:
Female
/
Humans
/
Infant
Language:
English
Journal:
J. investig. allergol. clin. immunol
Year:
2015
Document type:
Article
Institution/Affiliation country:
Kazusa DNA Research Institute/Japan
/
Shinshu University School of Medicine/Japan
/
Shinshu University/Japan