Bi-allelic Loss-of-Function Variants in DNMBP Cause Infantile Cataracts.
Am J Hum Genet
; 103(4): 568-578, 2018 10 04.
Article
in En
| MEDLINE
| ID: mdl-30290152
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genetic Variation
/
Cataract
/
Loss of Heterozygosity
/
Genetic Predisposition to Disease
/
Cytoskeletal Proteins
Type of study:
Prognostic_studies
Limits:
Adult
/
Animals
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Am J Hum Genet
Year:
2018
Type:
Article
Affiliation country:
Switzerland