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A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block

✍ Scribed by Tetsuo Kitaguchi; Shiro Matsubara; Masaru Sato; Kazuhito Miyamoto; Shunsaku Hirai; Ketty Schwartz; Gisèle Bonne

No coin nor oath required. For personal study only.

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