Bi-allelic variants in MDH2: Expanding the clinical phenotype.
Clin Genet
; 101(2): 260-264, 2022 02.
Article
in En
| MEDLINE
| ID: mdl-34766628
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phenotype
/
Genetic Predisposition to Disease
/
Alleles
/
Genetic Association Studies
/
Malate Dehydrogenase
/
Mutation
Type of study:
Prognostic_studies
Limits:
Child
/
Child, preschool
/
Humans
/
Infant
Language:
En
Journal:
Clin Genet
Year:
2022
Document type:
Article
Affiliation country:
Italy
Country of publication:
Denmark