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Q36733859-40FEC5E7-E7BE-4B15-8000-07E668E54E1F
Q36733859-40FEC5E7-E7BE-4B15-8000-07E668E54E1F
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http://www.wikidata.org/entity/statement/Q36733859-40FEC5E7-E7BE-4B15-8000-07E668E54E1F
Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11.
P2860
Q36733859-40FEC5E7-E7BE-4B15-8000-07E668E54E1F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36733859-40FEC5E7-E7BE-4B15-8000-07E668E54E1F
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wasDerivedFrom
e3b257075fd175094d1a0825d3280bd5d3ef90ee
P2860
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.