Mutations of the GPR179 Gene in Congenital Stationary Night Blindness

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United States of America Patent

APP PUB NO 20150031569A1
SERIAL NO

14373730

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ATTORNEY / AGENT: (SPONSORED)

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Abstract

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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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Patent Owner(s)

Patent OwnerAddress
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)101 RUE DE TOLBIAC PARIS 75013
UNIVERSITE PIERRE ET MARIE CURIE (PARIS 6)4 PLACE JUSSIEU PARIS 45005
CENTRE NATIONAL DE LA RECHERCHE MEDICALE3 RUE MICHEL ANGE PARIS F-75016

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Inventor(s)

Inventor Name Address # of filed Patents Total Citations
Audo, Isabelle Paris, FR 4 0
Jakowska, Kinga Paris, FR 1 0
Orhan, Elise Paris, FR 2 0
Sahel, Jose-Alain Paris, FR 39 165
Zeitz, Christina Paris, FR 3 1

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