Leandro Ucela Alves

Waardenburg syndrome: Novel mutations in a large Brazilian sample

Magnolia Astrid Pretell Bocángel, Uirá Souto Melo, Leandro Ucela Alves et al. · European Journal of Medical Genetics · 2018 · 38 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss

Vitor G.L. Dantas, Manmeet H. Raval, Ángela Ballesteros et al. · Scientific Reports · 2018 · 31 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

<i>NCOA3</i> identified as a new candidate to explain autosomal dominant progressive hearing loss

Rodrigo Salazar‐Silva, Vitor Lima Goes Dantas, Leandro Ucela Alves et al. · Human Molecular Genetics · 2020 · 21 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

A novel c.1037C &gt; G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome

Leandro Ucela Alves, Eliete Pardono, Paulo Alberto Otto et al. · Genetics and Molecular Biology · 2015 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family

Daniela Tiaki Uehara, Érika L. Freitas, Leandro Ucela Alves et al. · Human Genome Variation · 2015 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16