Study of Met34Thr variant in nonsyndromic hearing loss in four Portuguese families
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Biochemistry, Genetics and Molecular Biology
Reference26 articles.
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3. Molecular investigation of pediatric portuguese patients with sensorineural hearing loss.;Nogueira;Genet Res Int,2011
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1. Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis;Proceedings of the National Academy of Sciences;2020-11-23
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