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- Ek, MKarolinska Institutet (author)
Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders
- Article/chapterEnglish2023
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- 2023
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:152768867
- http://kipublications.ki.se/Default.aspx?queryparsed=id:152768867URI
- https://doi.org/10.3389/fneur.2023.1170005DOI
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- Language:English
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- Nilsson, DKarolinska Institutet (author)
- Engvall, M (author)
- Malmgren, HKarolinska Institutet (author)
- Thonberg, HKarolinska Institutet (author)
- Pettersson, MKarolinska Institutet (author)
- Anderlid, BMKarolinska Institutet (author)
- Hammarsjo, AKarolinska Institutet (author)
- Helgadottir, HTKarolinska Institutet (author)
- Arnardottir, S (author)
- Naess, K (author)
- Nennesmo, IKarolinska Institutet (author)
- Paucar, MKarolinska Institutet (author)
- Hjartarson, HT (author)
- Press, RKarolinska Institutet (author)
- Solders, G (author)
- Sejersen, TKarolinska Institutet (author)
- Lindstrand, AKarolinska Institutet (author)
- Kvarnung, MKarolinska Institutet (author)
- Karolinska Institutet (creator_code:org_t)
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- In:Frontiers in neurology14, s. 1170005-1664-2295
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