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Congenital Myasthenic Syndrome Caused by Novel Loss-of-Function Mutations in the Human AChR ɛ Subunit Gene

✍ Scribed by MARGHERITA MILONE; KINJI OHNO; TAKAYASU FUKUDOME; XIN-MING SHEN; ROBERT C. GRIGGS; ANDREW G. ENGEL

No coin nor oath required. For personal study only.

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