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Coppola Lab - GIFT Variant Database

LOVD v.3.0 Build 21 [ Current LOVD status ]
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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00002	FTD	Frontotemporal dementia	-	0	0	APP, C9orf72, CHMP2B, FUS, GRN, MAPT, PSEN1, PSEN2, TARDBP, TBK1, VCP	-	-