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Q24618126-3614B808-1640-4554-8B56-17C7680AF7F1
Q24618126-3614B808-1640-4554-8B56-17C7680AF7F1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24618126-3614B808-1640-4554-8B56-17C7680AF7F1
Structure and distribution of an Alu-type deletion mutation in Sandhoff disease
P2860
Q24618126-3614B808-1640-4554-8B56-17C7680AF7F1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24618126-3614B808-1640-4554-8B56-17C7680AF7F1
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wasDerivedFrom
a5b7b80a5b658bfac8ba7da132a34e152b6ff79f
P2860
AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2