Novel human pathological mutations. Gene symbol: GPR98. Disease: Usher syndrome 2C.
Hum Genet
; 125(3): 342, 2009 Apr.
Article
in En
| MEDLINE
| ID: mdl-19320012
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Sequence Deletion
/
Receptors, G-Protein-Coupled
/
Usher Syndromes
Limits:
Humans
Language:
En
Journal:
Hum Genet
Year:
2009
Document type:
Article
Affiliation country: