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Deciphering DST-associated disorders: biallelic variants affecting DST-b cause a congenital myopathy

Jacob, Maureen; Kölbel, Heike; Harrer, Philip; Kopajtich, Robert; Munot, Pinki; Achleitner, Melanie T; Badmann, Susann; ... Wagner, Matias; + view all (2025) Deciphering DST-associated disorders: biallelic variants affecting DST-b cause a congenital myopathy. Brain 10.1093/brain/awaf227. (In press).

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Type: Article
Title: Deciphering DST-associated disorders: biallelic variants affecting DST-b cause a congenital myopathy
Location: England
DOI: 10.1093/brain/awaf227
Publisher version: https://doi.org/10.1093/brain/awaf227
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher's terms and conditions.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
URI: https://discovery.ucl.ac.uk/id/eprint/10209957
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