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Q38745211-1DA60A32-1FCB-443B-B07D-8A23E79DC2AF
Q38745211-1DA60A32-1FCB-443B-B07D-8A23E79DC2AF
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http://www.wikidata.org/entity/statement/Q38745211-1DA60A32-1FCB-443B-B07D-8A23E79DC2AF
Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's disease.
P2860
Q38745211-1DA60A32-1FCB-443B-B07D-8A23E79DC2AF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38745211-1DA60A32-1FCB-443B-B07D-8A23E79DC2AF
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wasDerivedFrom
4aa97c734688c7ae3c2e2e1f362969d2de1b8561
P2860
Globotriaosylsphingosine (lyso-Gb3) might not be a reliable marker for monitoring the long-term therapeutic outcomes of enzyme replacement therapy for late-onset Fabry patients with the Chinese hotspot mutation (IVS4+919G>A).