Jekaterina Byčkova

Thiamine responsive megaloblastic anemia syndrome: A novel homozygous <i>SLC19A2</i> gene mutation identified

Violeta Mikštienė, Jurgita Songailienė, Jekaterina Byčkova et al. · American Journal of Medical Genetics Part A · 2015 · 30 citations

The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population

Violeta Mikštienė, Audronė Jakaitienė, Jekaterina Byčkova et al. · BMC Genetics · 2016 · 24 citations · Full text

Evaluation of quality of life after paediatric cochlear implantation

Jekaterina Byčkova, Justė Simonavičienė, Vaiva Mickevičienė et al. · Acta medica Lituanica · 2019 · 17 citations · Full text