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Publication Detail
The c.794C > T p.(Ala265Val) SCN4A variant may be associated with congenital myopathy with FSHD-like phenotype
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Publication Type:Conference presentation
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Authors:Plevova B, Zidkova J, Lassuthova P, Mannikko R, Haberlova J
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Date:01/04/2022
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Status:Published
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Language:English
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Keywords:Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Genetics & Heredity
Abstract
No abstract found
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