Open AccessCongenital myasthenic syndrome due to homozygous mutation of the cholinergic receptor nicotinic epsilon subunit in a Moroccan child
Author(s) -
M.A. Rafai,
M. Berrada,
Bouchra El Moutawakil,
Hicham El Otmani,
Hind Dehbi
Publication year - 2022
Publication title -
annales africaines de médecine
Language(s) - English
Resource type - Journals
eISSN - 2313-3589
pISSN - 2309-5784
DOI - 10.4314/aamed.v15i2.10
Subject(s) - congenital myasthenic syndrome , ptosis , acetylcholine receptor , nicotinic agonist , medicine , endocrinology , gynecology , receptor , surgery