Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Am J Hum Genet
; 101(5): 789-802, 2017 Nov 02.
Article
in En
| MEDLINE
| ID: mdl-29100090
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Congenital Abnormalities
/
Exome
/
Kidney
/
Kidney Diseases
/
Mutation
/
Neoplasm Proteins
Type of study:
Observational_studies
/
Risk_factors_studies
Limits:
Animals
/
Female
/
Humans
/
Male
Language:
En
Journal:
Am J Hum Genet
Year:
2017
Type:
Article