Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency.
Am J Hematol
; 95(5): 472-482, 2020 05.
Article
in En
| MEDLINE
| ID: mdl-32043619
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Pyruvate Kinase
/
Pyruvate Metabolism, Inborn Errors
/
Genetic Association Studies
/
Anemia, Hemolytic, Congenital Nonspherocytic
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
/
Middle aged
/
Newborn
Language:
En
Journal:
Am J Hematol
Year:
2020
Document type:
Article
Affiliation country:
Italia
Country of publication:
Estados Unidos