z-logo
open-access-imgOpen Access
Screening For Mutations In The Coding Regions Of PSEN1 Gene, 16-17 Exons Of APP Gene And APOE Genotyping In Patients With Alzheimer’s Disease
Author(s) -
Tuğçe Karaduman
Publication year - 2020
Publication title -
türk doğa ve fen dergisi :/türk doğa ve fen dergisi
Language(s) - English
Resource type - Journals
eISSN - 2149-6366
pISSN - 2147-303X
DOI - 10.46810/tdfd.713624
Subject(s) - psen1 , exon , genotype , apolipoprotein e , allele , allele frequency , genotyping , genetics , presenilin , alzheimer's disease , biology , gene , microbiology and biotechnology , medicine , disease

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom