Case report: Novel SCN4A variant associated with a severe congenital myasthenic syndrome/myopathy phenotype

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Case report: Novel SCN4A variant associated with a severe congenital myasthenic syndrome/myopathy phenotype

Author: Berghold, Veronika M.; Koko, Mahmoud; Berutti, Riccardo; Plecko, Barbara
Tübinger Autor(en):
Koko, Mahmoud
Published in: Frontiers in Pediatrics (2022), Bd. 10, Article 944784
Verlagsangabe: Frontiers Media Sa
Language: English
Full text: http://dx.doi.org/10.3389/fped.2022.944784
ISSN: 2296-2360
DDC Classifikation: 610 - Medicine and health
Dokumentart: Article
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