Salla Välipakka
4PUBLICATIONS
21CO-AUTHORS
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Publications (4)
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|Jan 29, 2025
A deep intronic PHEX variant associated with X-linked hypophosphatemia in a Finnish family.Laura Koponen, Minna Pekkinen, Jelmer Legebeke
|Sep 22, 2022
Adult-onset dominant muscular dystrophy in Greek families caused by Annexin A11.Mridul Johari, George Papadimas, Constantinos Papadopoulos
|Nov 01, 2021
Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene.Peter Hackman, Salla M Rusanen, Mridul Johari
|Mar 08, 2019
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild calf-predominant myopathy.Manu Jokela, Giorgio Tasca, Anna Vihola
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Frequent Collaborators
3 joint publications
Mridul Johari
3 joint publications
Marco Savarese
2 joint publications
Anna Vihola
2 joint publications
Per-Harald Jonson
2 joint publications
Bjarne Udd
1 joint publications
Peter Hackman
1 joint publications
Jaakko Sarparanta
1 joint publications
Kati Donner
1 joint publications
Ibrahim Mahjneh
1 joint publications
Mari Auranen
