Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency.
EMBO Mol Med
; 8(12): 1455-1469, 2016 12.
Article
in En
| MEDLINE
| ID: mdl-27861128
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Osteochondrodysplasias
/
Homeodomain Proteins
/
Genetic Predisposition to Disease
/
Cytochrome P450 Family 26
/
Growth Disorders
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Aged
/
Animals
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Year:
2016
Type:
Article