Glanzmann thrombasthenia in Pakistan: molecular analysis and identification of novel mutations.
Clin Genet
; 89(2): 187-92, 2016 Feb.
Article
in En
| MEDLINE
| ID: mdl-26096001
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Thrombasthenia
/
Mutation, Missense
Type of study:
Diagnostic_studies
/
Etiology_studies
/
Incidence_studies
/
Observational_studies
/
Prognostic_studies
/
Qualitative_research
/
Risk_factors_studies
Limits:
Adolescent
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
/
Newborn
Country/Region as subject:
Asia
Language:
En
Journal:
Clin Genet
Year:
2016
Document type:
Article