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Paper Details

The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects.
Genet Med
53
2018
11-exon macro-deletion, 7-exon, A1-42, Alzheimer, C9orf72, C9orf72 repeat, CHCHD10, CNV, CNVs, CTSF, CYP27A1, FTD, GRN, MAPT, MAPT mutations, PSEN1, PSEN2, SQSTM1, TARDBP, TBK1, UBQLN2, cholesterol, frontotemporal brain, frontotemporal dementia, macro, neurodegenerative disease, neurodegenerative disease genes, progranulin
Author NameAffiliation
Christian HaassBiomedical Center (BMC), Ludwig-Maximilians-Universitat Munchen
Christian HaassGerman Center for Neurodegenerative Diseases (DZNE) Munich
Christian Haass
Christian HaassBiomedical Center (BMC), Ludwig-Maximilians-Universitat Munchen
Christian Haass
Christian HaassGerman Center for Neurodegenerative Diseases (DZNE) Munich
Saskia BiskupCenter for Genomics and Transcriptomics
Patrizia RizzuGerman Center for Neurodegenerative Diseases (DZNE)
Peter HeutinkHertie Institute for Clinical Brain Research, University of Tubingen
Peter HeutinkGerman Center for Neurodegenerative Diseases (DZNE)
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