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Q47981703-B6117D6B-D290-4E2F-BC40-17718688FEFE
Q47981703-B6117D6B-D290-4E2F-BC40-17718688FEFE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47981703-B6117D6B-D290-4E2F-BC40-17718688FEFE
Complicated hereditary spastic paraplegia due to ATP13A2 mutations: what's in a name?
P2860
Q47981703-B6117D6B-D290-4E2F-BC40-17718688FEFE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47981703-B6117D6B-D290-4E2F-BC40-17718688FEFE
rank
NormalRank
type
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Statement
wasDerivedFrom
977b7e0f93ec7ca0dd8a657036faef59415dc0dc
P2860
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability