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Document type:
Zeitschriftenaufsatz
Author(s):
Berghold, Veronika M. ; Koko, Mahmoud ; Berutti, Riccardo ; Plecko, Barbara
Title:
Case report: Novel SCN4A variant associated with a severe congenital myasthenic syndrome/myopathy phenotype
Keywords:
Pediatrics ; Na ; loss of function (LOF) ; ion channel gene defect ; whole exome sequencing ; ion channels ; sodium channel paralogs ; genetic testing ; complex I deficiency
Journal title:
Frontiers in Pediatrics
Year:
2022
Journal volume:
10
Fulltext / DOI:
doi:10.3389/fped.2022.944784
Publisher:
Frontiers Media S.A.
E-ISSN:
2296-2360
Date of publication:
26.08.2022
CC license:
by, https://creativecommons.org/licenses/by/4.0
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