Congenital myasthenic syndrome: Correlation between clinical features and molecular diagnosis.
Estephan EP, Zambon AA, Thompson R, Polavarapu K, Jomaa D, Töpf A, Helito PVP, Heise CO, Moreno CAM, Silva AMS, Kouyoumdjian JA, Morita MDP, Reed UC, Lochmüller H, Zanoteli E.
Estephan EP, et al. Among authors: kouyoumdjian ja.
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Eur J Neurol. 2022.
PMID: 34749429