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Genome sequencing w...
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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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LIBRIS-ID:oai:prod.swepub.kib.ki.se:152768867
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http://kipublications.ki.se/Default.aspx?queryparsed=id:152768867URI
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https://doi.org/10.3389/fneur.2023.1170005DOI
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
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Nilsson, DKarolinska Institutet
(author)
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Engvall, M
(author)
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Malmgren, HKarolinska Institutet
(author)
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Thonberg, HKarolinska Institutet
(author)
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Pettersson, MKarolinska Institutet
(author)
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Anderlid, BMKarolinska Institutet
(author)
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Hammarsjo, AKarolinska Institutet
(author)
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Helgadottir, HTKarolinska Institutet
(author)
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Arnardottir, S
(author)
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Naess, K
(author)
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Nennesmo, IKarolinska Institutet
(author)
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Paucar, MKarolinska Institutet
(author)
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Hjartarson, HT
(author)
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Press, RKarolinska Institutet
(author)
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Solders, G
(author)
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Sejersen, TKarolinska Institutet
(author)
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Lindstrand, AKarolinska Institutet
(author)
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Kvarnung, MKarolinska Institutet
(author)
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Karolinska Institutet
(creator_code:org_t)
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In:Frontiers in neurology14, s. 1170005-1664-2295
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- By the author/editor
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Ek, M
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Nilsson, D
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Engvall, M
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Malmgren, H
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Thonberg, H
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Pettersson, M
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show more...
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Anderlid, BM
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Hammarsjo, A
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Helgadottir, HT
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Arnardottir, S
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Naess, K
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Nennesmo, I
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Paucar, M
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Hjartarson, HT
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Press, R
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Solders, G
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Sejersen, T
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Lindstrand, A
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Kvarnung, M
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Frontiers in neu ...
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Karolinska Institutet