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Q41840638-A839AC07-3DFA-4183-A48E-53DEF1C743DC
Q41840638-A839AC07-3DFA-4183-A48E-53DEF1C743DC
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http://www.wikidata.org/entity/statement/Q41840638-A839AC07-3DFA-4183-A48E-53DEF1C743DC
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy.
P2860
Q41840638-A839AC07-3DFA-4183-A48E-53DEF1C743DC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41840638-A839AC07-3DFA-4183-A48E-53DEF1C743DC
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wasDerivedFrom
4eaa37471ca4399302c8b11304f69a42854f9ee5
P2860
Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis