Associated Papers
Severe congenital myasthenic syndrome with novel variants in the CHRND gene.
Kondo H et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2022
Congenital myasthenic syndrome in Japan: ethnically unique mutations in muscle nicotinic acetylcholine receptor subunits.
Azuma Y et al.
Neuromuscular Disorders : Nmd, 2015
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