MUTATIONS OF THE GPR179 GENE IN CONGENITAL STATIONARY NIGHT BLINDNESS

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Dec 3, 2014
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Jan 23, 2013
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Jan 23, 2012

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Abstract

The present invention relates to an in vitro method for diagnosing a complete congenital stationary night blindness (cCSNB) in a subject, which method comprises determining the presence of an alteration in the GPR179 gene in a biological sample of said subject. Screening methods and therapeutic applications are further described.

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CENTRE NAT RECH SCIENT	FRPARIS FRA

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C12Q:MEASURING OR TESTING PROCESSES INVOLVING ENZYMES O....

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Inventor Name	Address
SAHEL JOSE-ALAIN	75013 PARIS
ZEITZ CHRISTINA	75012 PARIS
AUDO ISABELLE	ORSAY
ORHAN ELISE	RUEIL-MALMAISON
BUJAKOWSKA KINGA	F-75012 PARIS

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2807276

MUTATIONS OF THE GPR179 GENE IN CONGENITAL STATIONARY NIGHT BLINDNESS

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MUTATIONS OF THE GPR179 GENE IN CONGENITAL STATIONARY NIGHT BLINDNESS

European Patent Office Patent

13710028

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13710028

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