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Mutations in SCN4A: A Rare but Treatable Cau…
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SCN4A (Nav1.4) antibody - BiCell Scientific®
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SCN4A variants and SNV-based haplotype analysis for p.T1313M. A ...
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SCN4B Antibody - Cat. No. 18-…
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Anti-SCN4A antibody produced in rabbit Pre…
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What is SCN2A? - SCN2A Australia
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SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap ...
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SCN4A antibody (28315-1-AP) | Proteintech
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Nucleotide sequence analyses of the SCN4…
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Genetic code of the SCN4A gene. The poi…
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A novel missense variant of SCN4A co‐segregates with congenital ...
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Clinical features of patients with the SCN4A mutation | Download Table
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CACNA1S and SCN4A mutations in our study are pictured in the same ...
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A novel mutation in SCN4A causes severe myotonia and school-age-…
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