Biallelic variants in ASCC3 expand the phenotypic spectrum of congenital myasthenic syndromes

M. Johari, B. Herman, K. Polavarapu, A. Nalini, J. Lupski, A. Topf, M. Villanova, G. Tasca, E. Mercuri, E. Pegoraro, M. Sivasankar, Volker Straub, E. Malfatti, H. Lochmuller, D. Calame, G. Ravenscroft

Research output: Contribution to journalAbstract/Meeting Abstractpeer-review

Original languageEnglish
Article numberLBP.03
Number of pages1
JournalNeuromuscular Disorders
Volume32
Publication statusPublished - Oct 2022

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