Search Results - "Lundahl, Derek"

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  1. 1
    Expanding the phenotype of CACNA1C mutation disorders

    Expanding the phenotype of CACNA1C mutation disorders by Gakenheimer‐Smith, Lindsey, Meyers, Lindsay, Lundahl, Derek, Menon, Shaji C., Bunch, T. Jared, Sawyer, Briana L., Tristani‐Firouzi, Martin, Etheridge, Susan P.

    Published in Molecular genetics & genomic medicine (01-06-2021)
    “…Background Pathogenic variants in the L‐type Ca2+ channel gene CACNA1C cause a multi‐system disorder that includes severe long QT syndrome (LQTS), congenital…”
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    Abstract 16173: NFTAc1 is a Novel Atrial Fibrillation Susceptibility Gene

    Abstract 16173: NFTAc1 is a Novel Atrial Fibrillation Susceptibility Gene by Torres, Natalia S, Ferrel, Meganne, Jou, Chuanchau J, Arrington, Cammon B, Bowles, Neil E, Lundahl, Derek, Acuna, Alexandra, Shah, Karishma, Cho, Scott, Kauffman, Christopher, Yandell, Mark, Tristani-Firouzi, Martin

    Published in Circulation (New York, N.Y.) (19-11-2019)
    “…Atrial fibrillation (AF) is a common cardiac arrhythmia with a strong component of heritability. Genome-wide association and family studies have identified ion…”
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