APP c.423G>A ;(p.M141I)

Variant ID: 21-27425597-C-T

NM_000484.3(APP):c.423G>A;(p.M141I)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Subjects harboring presenilin familial Alzheimer's disease mutations exhibit diverse white matter biochemistry alterations.

American Journal Of Neurodegenerative Disease
Roher, Alex E AE; Maarouf, Chera L CL; Malek-Ahmadi, Michael M; Wilson, Jeffrey J; Kokjohn, Tyler A TA; Daugs, Ian D ID; Whiteside, Charisse M CM; Kalback, Walter M WM; Macias, Mimi P MP; Jacobson, Sandra A SA; Sabbagh, Marwan N MN; Ghetti, Bernardino B; Beach, Thomas G TG
Publication Date: 2013

Variant appearance in text: APP: M141I
PubMed Link: 24093083
Variant Present in the following documents:
  • Main text
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