Functional Characterization of a Novel Heterozygous Mutation in the Glucokinase Gene That Causes MODY2 in Chinese Pedigrees.
Front Endocrinol (Lausanne)
; 12: 803992, 2021.
Article
in En
| MEDLINE
| ID: mdl-34956103
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Asian People
/
Diabetes Mellitus, Type 2
/
Glucokinase
/
Heterozygote
/
Mutation
Type of study:
Etiology_studies
/
Observational_studies
/
Risk_factors_studies
Limits:
Adult
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Front Endocrinol (Lausanne)
Year:
2021
Document type:
Article
Affiliation country:
China