L. A. Virmond

A novel variant in the COX15 gene causing a fatal infantile cardioencephalomyopathy: a case report with clinical and molecular review.

F. Milanezi, C. Tengan, Eduardo Perrone, 2021, European journal of medical genetics.

Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes

M. Cervato, R. Guedes, Tatiana Ferreira de Almeida, 2022, Frontiers in Genetics.