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2052508
2052508
https://w3id.org/oc/corpus/br/2052508
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction
P3181
22092677be85893942961ef941d5e3354814f276
P3181
Q24336179-840F01AD-7941-443D-9F4D-9434C6E24B69
P3181
2052508
https://w3id.org/oc/corpus/br/2052508