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    Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH von Zhu, Na, Swietlik, Emilia, Welch, Carrie, Pauciulo, Michael, Hagen, Jacob, Zhou, Xueya, Guo, Yicheng, Karten, Johannes, Pandya, Divya, Tilly, Tobias, Lutz, Katie, Martin, Jennifer, Treacy, Carmen, Rosenzweig, Erika, Krishnan, Usha, Coleman, Anna, Gonzaga-Jauregui, Claudia, Lawrie, Allan, Trembath, Richard, Wilkins, Martin, Hirsch, Russel, White, R. James, Simon, Marc, Badesch, David, Burger, Charles, Chakinala, Murali, Thenappan, Thenappan, Elliott, Greg, Simms, Robert, Farber, Harrison, Frantz, Robert, Elwing, Jean, Hill, Nicholas, Ivy, Dunbar, Klinger, James, Nathan, Steven, Oudiz, Ronald, Robbins, Ivan, Schilz, Robert, Fortin, Terry, Wilt, Jeffrey, Yung, Delphine, Austin, Eric, Ahmad, Ferhaan, Bhatt, Nitin, Lahm, Tim, Frost, Adaani, Safdar, Zeenat, Rehman, Zia, Walter, Robert, Torres, Fernando, Bakshi, Sahil, Archer, Stephen, Argula, Rahul, Barnett, Christopher, Benza, Raymond, Desai, Ankit, Maddipati, Veeranna, Bogaard, Harm, Church, Colin, Coghlin, Gerry, Condliffe, Robin, Eyries, Mélanie, Gall, Henning, Ghio, Stefano, Girerd, Barbara, Holden, Simon, Howard, Luke, Humbert, Marc, Kiely, David, Kovacs, Gabor, Lordan, Jim, Machado, Rajiv, Mackenzie Ross, Robert, Mccabe, Colm, Moledina, Shahin, Montani, David, Olschewski, Horst, Penkett, Christopher, Pepke-Zaba, Joanna, Price, Laura, Rhodes, Christopher, Seeger, Werner, Soubrier, Florent, Southgate, Laura, Suntharalingam, Jay, Swift, Andrew, Toshner, Mark, Vonk Noordegraaf, Anton, Wharton, John, Wild, Jim, Wort, Stephen John, Eyries, Mélanie, Morrell, Nicholas, Shen, Yufeng, Gräf, Stefan, Nichols, William, Chung, Wendy

    Veröffentlicht in Genome medicine

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