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Q24336179-D20C5E9D-B488-46FD-8155-77E943A2E761
Q24336179-D20C5E9D-B488-46FD-8155-77E943A2E761
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Statement
http://www.wikidata.org/entity/statement/Q24336179-D20C5E9D-B488-46FD-8155-77E943A2E761
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction
P5008
Q24336179-D20C5E9D-B488-46FD-8155-77E943A2E761
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24336179-D20C5E9D-B488-46FD-8155-77E943A2E761
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P5008
ScienceSource