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Genotype–phenotype association in patients with SCN4A mutation – Authors' reply

Matthews, E; Männikkö, R; Behr, E; Hanna, MG; (2019) Genotype–phenotype association in patients with SCN4A mutation – Authors' reply. [Letter]. The Lancet , 393 (10188) pp. 2301-2302. 10.1016/S0140-6736(19)30214-4. Green open access

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Matthews_Genotype-phenotype association in patients with SCN4A mutation - Authors' reply_AAM.pdf - Accepted Version
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Type: Article
Title: Genotype–phenotype association in patients with SCN4A mutation – Authors' reply
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1016/S0140-6736(19)30214-4
Publisher version: https://doi.org/10.1016/S0140-6736(19)30214-4
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/10076070
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