z-logo
open-access-imgOpen Access
Congenital myasthenic syndrome due to homozygous mutation of the cholinergic receptor nicotinic epsilon subunit in a Moroccan child
Author(s) -
Mohammed Abdoh Rafai,
Malika Berrada,
Bouchra El Moutawakil,
Hicham El Otmani,
Hind Dehbi
Publication year - 2022
Publication title -
annales africaines de medecine
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

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom