Milla Laarne
5PUBLICATIONS
39CO-AUTHORS
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Publications (5)
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|Feb 16, 2026
Vacuolar myopathy caused by CASQ1 p.Asp244His: pathogenic evidence from two unrelated Chinese families.Xingyu Xia, Milla Laarne, Tonglin Pan
|Nov 28, 2025
Characterization of novel CASQ1 variants in two families with unusual phenotypic features.Milla Laarne, Manu Jokela, Fang Zhao
|Jun 14, 2025
Structural variation in nebulin and its impact on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions.Lydia Sagath, Kirsi Kiiski, Kireshnee Naidu
|May 21, 2025
A homozygous single-nucleotide variant in TNNT1 causes abnormal troponin T isoform expression in a patient with severe nemaline myopathy: A case report.Milla Laarne, Ali Oghabian, Jenni Laitila
|Jan 13, 2025
Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions.Lydia Sagath, Kirsi Kiiski, Kireshnee Naidu
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Frequent Collaborators
4 joint publications
Vilma-Lotta Lehtokari
4 joint publications
Katarina Pelin
3 joint publications
Lydia Sagath
2 joint publications
Kirsi Kiiski
2 joint publications
Alan H Beggs
2 joint publications
Per Harald Jonson
2 joint publications
Maureen Kelly Galindo
2 joint publications
Susan T Iannaccone
2 joint publications
Marco Savarese
1 joint publications
Krutik Patel
