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Q38626056-241A12B3-78F4-45DE-92C3-AB7B4BAB81CF
Q38626056-241A12B3-78F4-45DE-92C3-AB7B4BAB81CF
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http://www.wikidata.org/entity/statement/Q38626056-241A12B3-78F4-45DE-92C3-AB7B4BAB81CF
Epidemiology and molecular mechanism of frontotemporal lobar degeneration/amyotrophic lateral sclerosis with repeat expansion mutation in C9orf72.
P2860
Q38626056-241A12B3-78F4-45DE-92C3-AB7B4BAB81CF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38626056-241A12B3-78F4-45DE-92C3-AB7B4BAB81CF
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wasDerivedFrom
33f78d17a0445acda7dabb110429a1ba48cc50cf
P2860
C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population.