Expanding the phenotype of CACNA1C mutation disorders

por Gakenheimer‐Smith, Lindsey, Meyers, Lindsay, Lundahl, Derek, Menon, Shaji C., Bunch, T. Jared, Sawyer, Briana L., Tristani‐Firouzi, Martin, Etheridge, Susan P.
Publicado 2021

The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele

por Hateley, Shannon, Lopez-Izquierdo, Angelica, Jou, Chuanchau J., Cho, Scott, Schraiber, Joshua G., Song, Shiya, Maguire, Colin T., Torres, Natalia, Riedel, Michael, Bowles, Neil E., Arrington, Cammon B., Kennedy, Brett J., Etheridge, Susan P., Lai, Shuping, Pribble, Chase, Meyers, Lindsay, Lundahl, Derek, Byrnes, Jake, Granka, Julie M., Kauffman, Christopher A., Lemmon, Gordon, Boyden, Steven, Scott Watkins, W., Karren, Mary Anne, Knight, Stacey, Brent Muhlestein, J., Carlquist, John F., Anderson, Jeffrey L., Chahine, Kenneth G., Shah, Khushi U., Ball, Catherine A., Benjamin, Ivor J., Yandell, Mark, Tristani-Firouzi, Martin
Publicado 2021