A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with ß-Thalassemia Trait Results in Severe Hemolytic Anemia.
Hemoglobin
; 43(2): 77-82, 2019 Mar.
Article
in En
| MEDLINE
| ID: mdl-31190578
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Homozygote
/
Mutation
Limits:
Child, preschool
/
Humans
/
Male
Language:
En
Journal:
Hemoglobin
Year:
2019
Type:
Article
Affiliation country:
Netherlands