The role of ATP9A (c.1091G > C; p.(Arg364Thr)) variant in cognitive impairment: diagnostic insight from whole exome sequencing

Molecular Biology Reports 2026

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Authors: Cuneyd Yavas, Asmaa Abuaısha, Emir Nekay, Alper Gezdirici, Halil Ibrahim Yilmaz, Ekrem Akbulut, Pinar Arican
DOI: 10.1007/s11033-026-11496-5
Cited by: 2
References: 28

Fields of Study & Subjects

Genomics and Rare Diseases Genomic variations and chromosomal abnormalities Hereditary Neurological Disorders

Publication details

Journal / source
Molecular Biology Reports
Publisher
Springer Science and Business Media LLC
Volume
53
Issue
1
Pages
329–329
Publication date
28 January 2026
Language
EN