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Q24336179-8A8FF726-0C8F-477A-A19E-22C751DB8C19
Q24336179-8A8FF726-0C8F-477A-A19E-22C751DB8C19
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Statement
http://www.wikidata.org/entity/statement/Q24336179-8A8FF726-0C8F-477A-A19E-22C751DB8C19
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction
P2860
Q24336179-8A8FF726-0C8F-477A-A19E-22C751DB8C19
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24336179-8A8FF726-0C8F-477A-A19E-22C751DB8C19
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wasDerivedFrom
92354d40c3286da652b0ca784392ce8190418d5b
P2860
Suppression of autophagy permits successful enzyme replacement therapy in a lysosomal storage disorder--murine Pompe disease.