Malin Kvarnung
3PUBLICATIONS
9CO-AUTHORS
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Publications (3)
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|Nov 25, 2024
A Novel Type of Autosomal Dominant Episodic Nystagmus Segregating with a Variant in the FRMD5 Gene.Björn Hammar, Sofia Paulsson, Hafdis T Helgadottir
|Nov 30, 2023
Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3.Ilan Ben-Shabat, Malin Kvarnung, Wolfgang Sperker
|Sep 18, 2018
Genomic screening in rare disorders: New mutations and phenotypes, highlighting ALG14 as a novel cause of severe intellectual disability.Malin Kvarnung, Fulya Taylan, Daniel Nilsson
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Frequent Collaborators
1 joint publications
Fulya Taylan
1 joint publications
Ilan Ben-Shabat
1 joint publications
Wolfgang Sperker
1 joint publications
Anna Wredenberg
1 joint publications
Rolf Wibom
1 joint publications
Inger Nennesmo
1 joint publications
Martin Paucar
1 joint publications
Sofia Paulsson
1 joint publications
Hafdis T Helgadottir
