Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C.
Mol Vis
; 13: 1862-5, 2007 Oct 02.
Article
in En
| MEDLINE
| ID: mdl-17960123
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Myosins
/
Dyneins
/
Usher Syndromes
/
Mutation
Type of study:
Prognostic_studies
Limits:
Adult
/
Female
/
Humans
/
Male
Country/Region as subject:
Africa
Language:
En
Journal:
Mol Vis
Journal subject:
BIOLOGIA MOLECULAR
/
OFTALMOLOGIA
Year:
2007
Document type:
Article
Affiliation country:
Morocco