Search Results - Margarita Sharova

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    Case Report: New phenotype of late-onset Stüve-Wiedemann syndrome due to a C-terminal variant in the LIFR gene by Evgenia Melnik, Margarita Sharova, Vladimir Kenis, Anna Morgul, Viktoria Zabnenkova, Tatiana Markova

    Published 2024
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    Recessive myotonia congenita caused by a homozygous splice site variant in CLCN1 gene: a case report by Peter Sparber, Margarita Sharova, Alexandra Filatova, Olga Shchagina, Evgeniya Ivanova, Elena Dadali, Mikhail Skoblov

    Published 2020
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