EIF2AK3 variants in Dutch patients with Alzheimer's disease
Next-generation sequencing has contributed to our understanding of the genetics of Alzheimer's disease (AD) and has explained a substantial part of the missing heritability of familial AD. We sequenced 19 exomes from 8 Dutch families with a high AD burden and identified EIF2AK3, encoding for pr...
Main Authors: | Wong, T, Van Der Lee, S, Van Rooij, J, Meeter, L, Frick, P, Melhem, S, Seelaar, H, Ikram, M, Rozemuller, A, Holstege, H, Hulsman, M, Uitterlinden, A, Neumann, M, Hoozemans, J, Van Duijn, C, Rademakers, R, Van Swieten, J |
---|---|
Format: | Journal article |
Language: | English |
Published: |
Elsevier
2018
|
Similar Items
-
Mapping the genetic landscape of early-onset Alzheimer’s disease in a cohort of 36 families
by: Merel O. Mol, et al.
Published: (2022-06-01) -
Content expectations and dropout in Dutch vocational education
by: Irene Eegdeman, et al.
Published: (2020-10-01) -
Re : EIF2AK3 mutations in patients with Wolcott-Rallison syndrome.
by: Taha Doris
Published: (2005-01-01) -
Cognitive skills, personality traits and dropout in Dutch vocational education
by: Irene Eegdeman, et al.
Published: (2018-10-01) -
Pulmonary capillary hemangiomatosis: a focus on the EIF2AK4 mutation in onset and pathogenesis
by: Ma L, et al.
Published: (2015-08-01)