http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2019352624-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9d0e1705700a059b200c774b76ce1234
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-009
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Y301-06001
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-16
filingDate 2018-02-05^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3eda824ce50aa60b7c2941b47ffaa36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bbf953da628e0d5c6d8740ecc02efcf2
publicationDate 2019-11-21^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2019352624-A1
titleOfInvention Mutated arylsulfatase a
abstract The present invention pertains to a novel treatment of pathologies caused by an increased synthesis or accumulation of sulfolipids such as sulfatide. The invention provides mutated arylsulfatase A (ARSA or ASA, EC 3.1.6.8) enzymes with increased activity towards sulfatide metabolization. The invention provides nucleic acids encoding the mutant ARSA, the use of the proteins and nucleic acids, as well as pharmaceutical compositions comprising them, in the treatment of lysosomal storage disorders (LSDs) such as metachromatic leukodystrophy (MLD).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2023113806-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11459550-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022221193-A1
priorityDate 2017-02-03^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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