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Q24336179-C63A160F-3B52-4A60-A61C-4A7E85244E14
Q24336179-C63A160F-3B52-4A60-A61C-4A7E85244E14
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http://www.wikidata.org/entity/statement/Q24336179-C63A160F-3B52-4A60-A61C-4A7E85244E14
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction
P2860
Q24336179-C63A160F-3B52-4A60-A61C-4A7E85244E14
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24336179-C63A160F-3B52-4A60-A61C-4A7E85244E14
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wasDerivedFrom
92354d40c3286da652b0ca784392ce8190418d5b
P2860
Loss of sorting nexin 27 contributes to excitatory synaptic dysfunction by modulating glutamate receptor recycling in Down's syndrome.