D. Pelnena

Effects of a Mutation in the HSPE1 Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental Disorder

Joshua L. Deignan, P. Bross, A. Azem, 2016, Front. Mol. Biosci..

A New Baltic Population-Specific Human Genetic Marker in the PMCA4 Gene

M. Punab, A. Khrunin, S. Limborska, 2017, Human Heredity.

EAST/SeSAME syndrome: Review of the literature and introduction of four new Latvian patients

S. Kušķe, I. Inashkina, I. Micule, 2018, Clinical genetics.

Complete mtDNA sequencing reveals mutations m.9185T>C and m.13513G>A in three patients with Leigh syndrome

Z. Krūmiņa, L. Pliss, Evelina Dagytė, 2018, Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis.