Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection

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United States of America Patent

PATENT NO 9868989
APP PUB NO 20160076101A1
SERIAL NO

14858666

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Abstract

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A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.

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INSTITUT PASTEUR75724 PARIS CEDEX 15

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Inventor(s)

Inventor Name Address # of filed Patents Total Citations
Denoyelle-Gryson, Francoise Arcueil, FR 4 11
Guesdon, Jean-Luc Sevres, FR 25 350
Marlin, Sandrine La Garenne-Colombes, FR 2 0
Petit, Christine Le Plessis-Robinson, FR 20 32
Weil, Dominique Paris, FR 8 15

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