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Q34941895-953FC32C-C102-476C-9CCF-E54A91FD5A55
Q34941895-953FC32C-C102-476C-9CCF-E54A91FD5A55
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34941895-953FC32C-C102-476C-9CCF-E54A91FD5A55
Glycosphingolipid lysosomal storage diseases: therapy and pathogenesis.
P2860
Q34941895-953FC32C-C102-476C-9CCF-E54A91FD5A55
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34941895-953FC32C-C102-476C-9CCF-E54A91FD5A55
rank
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type
BestRank
Statement
wasDerivedFrom
fb8c203d9ec5f28e334348dc198232a1476bdf27
P2860
Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease