Kristiina Avela
3PUBLICATIONS
3CO-AUTHORS
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Publications (3)
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|Sep 21, 2022
Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG.Anna Majander, Eeva-Marja Sankila, Aura Falck
|May 16, 2019
The genetic aetiology of retinal degeneration in children in Finland - new founder mutations identified.Kristiina Avela, Riitta Salonen-Kajander, Arja Laitinen
|Oct 26, 2017
A founder mutation in CERKL is a major cause of retinal dystrophy in Finland.Kristiina Avela, Eeva-Marja Sankila, Sanna Seitsonen
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