P236: Leveraging automated tertiary analysis for exome sequencing in hereditary hearing loss: A pilot study

Genetics in Medicine Open 2026 Open access

Read full text
Authors: Mahnaz Norouzi, Erfan Khoram, Ladan Sadeghian, Mohammad Reza Pourreza, Mateusz Dawidziuk, Mateusz Marynowski, Klaudia Pacewicz, Marcin Piechota, Mohammad Amin Tabatabaiefar
DOI: 10.1016/j.gimo.2026.103730
Cited by: 0

Fields of Study & Subjects

Hearing Cochlea Tinnitus Genetics Genomics and Rare Diseases Congenital Ear and Nasal Anomalies

Publication details

Journal / source
Genetics in Medicine Open
Volume
4
Pages
103730–103730
Publication date
1 January 2026
Language
EN