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Q36733859-5CF38FD9-E931-48A6-BE6F-7A031AADBB39
Q36733859-5CF38FD9-E931-48A6-BE6F-7A031AADBB39
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http://www.wikidata.org/entity/statement/Q36733859-5CF38FD9-E931-48A6-BE6F-7A031AADBB39
Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11.
P2860
Q36733859-5CF38FD9-E931-48A6-BE6F-7A031AADBB39
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36733859-5CF38FD9-E931-48A6-BE6F-7A031AADBB39
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wasDerivedFrom
e3b257075fd175094d1a0825d3280bd5d3ef90ee
P2860
Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.