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Title:
IDENTIFICATION OF NEURAL DEFECTS ASSOCIATED WITH THE GENE
Document Type and Number:
WIPO Patent Application WO2001085995
Kind Code:
A9
Abstract:
A method for screening neural system defects in a human comprises: (A) providing chromosomal material from the human; (B) detecting a modification of the NAP1L2 gene in the chromosomal material, wherein the modification is selected from a) substitution, b) dele-tion, c) frame-shift, or d) insertion that causes a loss of biological function in the NAP1L2 gene; and (C) correlating the modification of the gene with a potential for a neural system defect. The method can also be practiced with the mouseNap1L2 gene.

Inventors:
AVNER PHILIP (FR)
ROGNER UTE CHRISTINE (FR)
SPYROPOULOS DEMETRI (US)
ROUGEULLE CLAIRE (FR)
Application Number:
PCT/IB2001/000960
Publication Date:
August 15, 2002
Filing Date:
May 04, 2001
Export Citation:
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Assignee:
PASTEUR INSTITUT (FR)
CENTRE NAT RECH SCIENT (FR)
AVNER PHILIP (FR)
ROGNER UTE CHRISTINE (FR)
SPYROPOULOS DEMETRI (US)
ROUGEULLE CLAIRE (FR)
International Classes:
G01N33/48; A61K45/00; A61P25/00; A61P35/00; C12N5/10; C12N15/09; C12Q1/68; C12Q1/6883; G01N33/15; G01N33/50; G01N33/53; (IPC1-7): C12Q1/68
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