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Q38745211-6D0291C0-752D-4264-9BC4-EBE51CBFC0E1
Q38745211-6D0291C0-752D-4264-9BC4-EBE51CBFC0E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38745211-6D0291C0-752D-4264-9BC4-EBE51CBFC0E1
Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's disease.
P2860
Q38745211-6D0291C0-752D-4264-9BC4-EBE51CBFC0E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38745211-6D0291C0-752D-4264-9BC4-EBE51CBFC0E1
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type
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wasDerivedFrom
4aa97c734688c7ae3c2e2e1f362969d2de1b8561
P2860
Uncertain diagnosis of fabry disease in patients with neuropathic pain, angiokeratoma or cornea verticillata: consensus on the approach to diagnosis and follow-up