GC c.1050_1057del ;(p.S351Dfs*10)

Variant ID: 4-72620802-CTTCTGCTT-C

NM_000583.3(GC):c.1050_1057del;(p.S351Dfs*10)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease.

Acta Neuropathologica
Verheijen, Jan J; Van den Bossche, Tobi T; van der Zee, Julie J; Engelborghs, Sebastiaan S; Sanchez-Valle, Raquel R; Lladó, Albert A; Graff, Caroline C; Thonberg, Håkan H; Pastor, Pau P; Ortega-Cubero, Sara S; Pastor, Maria A MA; Benussi, Luisa L; Ghidoni, Roberta R; Binetti, Giuliano G; Clarimon, Jordi J; Lleó, Alberto A; Fortea, Juan J; de Mendonça, Alexandre A; Martins, Madalena M; Grau-Rivera, Oriol O; Gelpi, Ellen E; Bettens, Karolien K; Mateiu, Ligia L; Dillen, Lubina L; Cras, Patrick P; De Deyn, Peter P PP; Van Broeckhoven, Christine C; Sleegers, Kristel K
Publication Date: 2016-08

Variant appearance in text: GC: 1050_1057del
PubMed Link: 27026413
Variant Present in the following documents:
  • Main text
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