Kristiina Avela

Years Active: 2017-2022
Publications (10 Years): 3

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

Publications

Anna Majander, Eeva-Marja Sankila, Aura Falck, Laura Kristiina Vasara, Sanna Seitsonen, Maarit Kulmala, Anna-Kaisa Haavisto, Kristiina Avela, Joni Antero Turunen
Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG. Acta ophthalmologica (2022)
Kristiina Avela, Riitta Salonen-Kajander, Arja Laitinen, Simon Ramsden, Stephanie Barton, Sirkka-Liisa Rudanko
The genetic aetiology of retinal degeneration in children in Finland - new founder mutations identified. Acta ophthalmologica 97 (8) (2019)
Kristiina Avela, Eeva-Marja Sankila, Sanna Seitsonen, Liina Kuuluvainen, Stephanie Barton, Stuart Gillies, Kristiina Aittomäki
A founder mutation in CERKL is a major cause of retinal dystrophy in Finland. Acta ophthalmologica 96 (2) (2017)

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