about
Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene.Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationA pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease.
P50
description
researcher ORCID ID = 0000-0003-4503-4717
@en
wetenschapper
@nl
name
Håkan Thonberg
@ast
Håkan Thonberg
@en
Håkan Thonberg
@nl
type
label
Håkan Thonberg
@ast
Håkan Thonberg
@en
Håkan Thonberg
@nl
prefLabel
Håkan Thonberg
@ast
Håkan Thonberg
@en
Håkan Thonberg
@nl
P106
P31
P496
0000-0003-4503-4717