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  1. 1
    Functional Study of Novel Bartter's Syndrome Mutations in ClC-Kb and Rescue by the Accessory Subunit Barttin Toward Personalized Medicine

    Functional Study of Novel Bartter's Syndrome Mutations in ClC-Kb and Rescue by the Accessory Subunit Barttin Toward Personalized Medicine von Sahbani, Dalila, Strumbo, Bice, Tedeschi, Silvana, Conte, Elena, Camerino, Giulia Maria, Benetti, Elisa, Montini, Giovanni, Aceto, Gabriella, Procino, Giuseppe, Imbrici, Paola, Liantonio, Antonella

    Veröffentlicht in Frontiers in pharmacology

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  2. 2
    The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C‐terminal peptide of the ClC‐1 channel

    The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C‐terminal peptide of the ClC‐1 channel von Altamura, Concetta, Lucchiari, Sabrina, Sahbani, Dalila, Ulzi, Gianna, Comi, Giacomo P., D'Ambrosio, Paola, Petillo, Roberta, Politano, Luisa, Vercelli, Liliana, Mongini, Tiziana, Dotti, Maria Teresa, Cardani, Rosanna, Meola, Giovanni, Lo Monaco, Mauro, Matthews, Emma, Hanna, Michael G., Carratù, Maria Rosaria, Conte, Diana, Imbrici, Paola, Desaphy, Jean‐François

    Veröffentlicht in Human mutation

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