Visual impairment and progressive phthisis bulbi caused by recessive pathogenic variant in MARK3.
Hum Mol Genet
; 27(15): 2703-2711, 2018 08 01.
Article
in En
| MEDLINE
| ID: mdl-29771303
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Vision Disorders
/
Protein Serine-Threonine Kinases
/
Eye Diseases
Limits:
Animals
/
Female
/
Humans
/
Male
Language:
En
Journal:
Hum Mol Genet
Year:
2018
Document type:
Article