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Volumn 5, Issue , 2015, Pages

Whole-exome sequencing identifies OR2W3 mutation as a cause of autosomal dominant retinitis pigmentosa

Author keywords

[No Author keywords available]

Indexed keywords

OLFACTORY RECEPTOR; OR2W3 PROTEIN, HUMAN;

EID: 84924964461     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep09236     Document Type: Article
Times cited : (25)

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