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Q46058379-5817E159-389D-41CB-9AC6-E462844B7F3A
Q46058379-5817E159-389D-41CB-9AC6-E462844B7F3A
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Statement
http://www.wikidata.org/entity/statement/Q46058379-5817E159-389D-41CB-9AC6-E462844B7F3A
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects.
P2860
Q46058379-5817E159-389D-41CB-9AC6-E462844B7F3A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46058379-5817E159-389D-41CB-9AC6-E462844B7F3A
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wasDerivedFrom
5a566c141fc3ffddfab0ec886f53d7b3eabb83cd
P2860
The role of individual domains and the significance of shedding of ATP6AP2/(pro)renin receptor in vacuolar H(+)-ATPase biogenesis.