Reticular dysgenesis: a very rare and fatal immunodeficiency disease
Alexandria Journal of Pediatrics. 2009; 23 (2): 19-22
in En
| IMEMR
| ID: emr-145774
Responsible library:
EMRO
Search on Google
Index:
IMEMR
Main subject:
Phenotype
/
Adenylate Kinase
/
Consanguinity
Type of study:
Case_reports
Limits:
Humans
/
Male
Language:
En
Journal:
Alex. J. Pediatr.
Year:
2009