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MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY

Known as: CMS1E, FORMERLY, MYASTHENIC SYNDROME, CONGENITAL, Ie, FORMERLY, CMS11 
National Institutes of Health

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6 relations
Autosomal recessive inheritanceBlepharoptosisByzanthine arch palateDecreased fetal movement

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