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Clinical characterization and genetic analysis of Korean patients with X-linked Charcot-Marie-Tooth disease type 1.
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- Journal of the Peripheral Nervous System, 2017, v. 22, n. 3, p. 172, doi. 10.1111/jns.12217
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A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.
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- Journal of the Peripheral Nervous System, 2014, v. 19, n. 2, p. 175, doi. 10.1111/jns5.12062
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- Article