Targeted next generation sequencing for molecular diagnosis of Usher syndrome.
Orphanet J Rare Dis
; 9: 168, 2014 Nov 18.
Article
in En
| MEDLINE
| ID: mdl-25404053
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Usher Syndromes
/
High-Throughput Nucleotide Sequencing
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Orphanet J Rare Dis
Journal subject:
MEDICINA
Year:
2014
Document type:
Article
Affiliation country:
Spain
Country of publication:
United kingdom