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Q35701678-EF3FBD60-1305-4402-B572-5FA84D3BA538
Q35701678-EF3FBD60-1305-4402-B572-5FA84D3BA538
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35701678-EF3FBD60-1305-4402-B572-5FA84D3BA538
Small-molecule enhancers of autophagy modulate cellular disease phenotypes suggested by human genetics.
P2860
Q35701678-EF3FBD60-1305-4402-B572-5FA84D3BA538
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35701678-EF3FBD60-1305-4402-B572-5FA84D3BA538
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wasDerivedFrom
f88fa2d273cd8ed6eb0708cde17229d9e40d3c78
P2860
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction