Independent origin of c.57 C > T mutation in MIR184 associated with inherited corneal and lens abnormalities.
Ophthalmic Genet
; 36(1): 95-7, 2015 Mar.
Article
in En
| MEDLINE
| ID: mdl-25373792
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Cataract
/
Germ-Line Mutation
/
Polymorphism, Single Nucleotide
/
MicroRNAs
/
White People
/
Keratoconus
Type of study:
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Ophthalmic Genet
Journal subject:
GENETICA MEDICA
/
OFTALMOLOGIA
Year:
2015
Document type:
Article
Affiliation country:
Estados Unidos
Country of publication:
Reino Unido