Clinical and molecular characterization of myotonia congenita using whole-exome sequencing in Egyptian patients
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s11033-024-09646-8.pdf
Reference52 articles.
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2. Stunnenberg BC, LoRusso S, Arnold WD et al (2020) Guidelines on clinical presentation and management of nondystrophic myotonias. Muscle Nerve 62:430–444
3. Chapman AM, Schurer M, Weijers L et al (2021) Improving the understanding of how patients with non-dystrophic myotonia are selected for myotonia treatment with mexiletine (NaMuscla): outcomes of treatment impact using a European Delphi panel. BMC Neurol 21:467. https://doi.org/10.1186/s12883-021-02491-3
4. Jitpimolmard N, Matthews E, Fialho D (2020) treatment updates for neuromuscular channelopathies. Curr Treat Opti Neurol 22:34. https://doi.org/10.1007/s11940-020-00644-2
5. Elizabeth S. Bryan; Mahdi Alsaleem (2022). Myotonia Congenita, StatPearls [Internet] Treasure Island (FL): StatPearls Publishing; Aug 29. PMID: 32966006, Bookshelf ID: NBK562335
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