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filingDate 2001-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2001-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-0164747-A1
titleOfInvention Mutations in spink5 responsible for netherton's syndrome and atopic diseases
abstract The invention relates to the identification of the SPINK5 gene as the gene which is mutated in the autosomal recessive genetic skin condition Netherton's Syndrome and as a susceptibility gene for atopic disease in general. Genetic screens, therapeutic products and Nucleic acids and proteins corresponding to mutant versions of the SPINK5 cDNA and expression product are all described.
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP71276
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ06SH2
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP21948
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ7CIZ3
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP61879
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP70753
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5959
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP61880
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCC0HJI1
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ60HF6

Total number of triples: 648.