Kediha_2023_Rev.Neurol.(Paris)__

Reference

Title : Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families - Kediha_2023_Rev.Neurol.(Paris)__
Author(s) : Kediha MI , Tazir M , Magnouche C , Sternberg D , Belarbi S , Eymard B , Ali Pacha L
Ref : Rev Neurol (Paris) , : , 2023
Abstract : Kediha_2023_Rev.Neurol.(Paris)__
ESTHER : Kediha_2023_Rev.Neurol.(Paris)__
PubMedSearch : Kediha_2023_Rev.Neurol.(Paris)__
PubMedID: 36764859

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Citations formats

Kediha MI, Tazir M, Magnouche C, Sternberg D, Belarbi S, Eymard B, Ali Pacha L (2023)
Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families
Rev Neurol (Paris) :

Kediha MI, Tazir M, Magnouche C, Sternberg D, Belarbi S, Eymard B, Ali Pacha L (2023)
Rev Neurol (Paris) :