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Q34941895-EAD5EA0D-72D3-41DA-828B-54B07E6AB177
Q34941895-EAD5EA0D-72D3-41DA-828B-54B07E6AB177
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34941895-EAD5EA0D-72D3-41DA-828B-54B07E6AB177
Glycosphingolipid lysosomal storage diseases: therapy and pathogenesis.
P2860
Q34941895-EAD5EA0D-72D3-41DA-828B-54B07E6AB177
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34941895-EAD5EA0D-72D3-41DA-828B-54B07E6AB177
rank
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type
BestRank
Statement
wasDerivedFrom
fb8c203d9ec5f28e334348dc198232a1476bdf27
P2860
Fabry disease: preclinical studies demonstrate the effectiveness of alpha-galactosidase A replacement in enzyme-deficient mice.