A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

Overview of attention for article published in Human Genetics, December 2006

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Retinitis pigmentosa GTPase regulator

Cited by user Boghog on 31 Dec 2020

X-linked retinitis pigmentosa GTPase regulator is a GTPase-binding protein that in humans is encoded by the RPGR gene.

Whirlina

Cited by user Señor Aluminio on 29 Dec 2010

DFNB31

Cited by user ProteinBoxBot on 20 Dec 2007

Whirlin is a protein that in humans is encoded by the DFNB31 gene.