Vilma-Lotta Lehtokari

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 2

Top Topics

Density Functional Theory

Mitochondrial Dna

Intellectual Disability

Top Venues

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Vilma-Lotta Lehtokari, Minna Similä, Marianne Tammepuu, Carina Wallgren-Pettersson, Sonja Strang-Karlsson, Sinikka Hiekkala
Self-reported functioning among patients with ultra-rare nemaline myopathy or a related disorder in Finland: a pilot study. Orphanet journal of rare diseases 18 (1) (2023)
Lydia Sagath, Vilma-Lotta Lehtokari, Katarina Pelin, Kirsi Kiiski
Array Comparative Genomic Hybridisation and Droplet Digital PCR Uncover Recurrent Copy Number Variation of the TTN Segmental Duplication Region. Genes 13 (5) (2022)