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Q47190201-9A7ECC20-2B6D-4635-8496-BECEE0A65CE1
Q47190201-9A7ECC20-2B6D-4635-8496-BECEE0A65CE1
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http://www.wikidata.org/entity/statement/Q47190201-9A7ECC20-2B6D-4635-8496-BECEE0A65CE1
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency.
P2860
Q47190201-9A7ECC20-2B6D-4635-8496-BECEE0A65CE1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47190201-9A7ECC20-2B6D-4635-8496-BECEE0A65CE1
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wasDerivedFrom
33bb1aeac69c4ba6272ee9b1749ca2e523d6727a
P2860
Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.