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inherited neuropathies consortium rare diseases clinical research network[Corporate Author]
(3 results)?
Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study.
Brain. 2020 Dec 1;143(12):3589-3602. doi: 10.1093/brain/awaa323.
Brain. 2020.
PMID: 33415332
Free PMC article.
Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants.
Record CJ, Skorupinska M, Laura M, Rossor AM, Pareyson D, Pisciotta C, Feely SME, Lloyd TE, Horvath R, Sadjadi R, Herrmann DN, Li J, Walk D, Yum SW, Lewis RA, Day J, Burns J, Finkel RS, Saporta MA, Ramchandren S, Weiss MD, Acsadi G, Fridman V, Muntoni F, Poh R, Polke JM, Zuchner S, Shy ME, Scherer SS, Reilly MM; Inherited Neuropathies Consortium—Rare Disease Clinical Research Network.
Record CJ, et al.
Brain. 2023 Oct 3;146(10):4336-4349. doi: 10.1093/brain/awad187.
Brain. 2023.
PMID: 37284795
Free PMC article.
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