Identification of a rare presenilin 1 single amino acid deletion mutation (F175del) with unusual amyloid-β processing effects-Reference-Cited by-同舟云学术

Identification of a rare presenilin 1 single amino acid deletion mutation (F175del) with unusual amyloid-β processing effects

Published:2019-12 Issue: Volume:84 Page:241.e5-241.e11
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Vöglein Jonathan,Willem Michael,Trambauer Johannes,Schönecker Sonja,Dieterich Marianne,Biskup Saskia,Giudici Camilla,Utz Kathrin,Oberstein Timo,Brendel Matthias^ORCID,Rominger Axel,Danek Adrian^ORCID,Steiner Harald,Haass Christian,Levin Johannes^ORCID

Funder

DFG; German Research Foundation)

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

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