학술논문

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH
Document Type
Article
Author
Zhu, N.Welch, C.L.Hagen, J.J.Zhou, X.Rosenzweig, E.B.Krishnan, U.Chung, W.K.Guo, Y.Shen, Y.Swietlik, E.M.Pandya, D.Tilly, T.Martin, J.M.Treacy, C.M.Morrell, N.W.Gräf, S.Pauciulo, M.W.Lutz, K.A.Coleman, A.W.Nichols, W.C.Karten, J.Lawrie, A.Trembath, R.C.Wilkins, M.R.Hirsch, R.White, R.J.Simon, M.Badesch, D.Rosenzweig, E.Burger, C.Chakinala, M.Thenappan, T.Elliott, G.Simms, R.Farber, H.Frantz, R.Elwing, J.Hill, N.Ivy, D.Klinger, J.Nathan, S.Oudiz, R.Robbins, I.Schilz, R.Fortin, T.Wilt, J.Yung, D.Austin, E.Ahmad, F.Bhatt, N.Lahm, T.Frost, A.Safdar, Z.Rehman, Z.Walter, R.Torres, F.Bakshi, S.Archer, S.Argula, R.Barnett, C.Benza, R.Desai, A.Maddipati, V.Bogaard, H.J.Church, C.Coghlin, G.Condliffe, R.Eyries, M.Gall, H.Ghio, S.Girerd, B.Holden, S.Howard, L.Humbert, M.Kiely, D.G.Kovacs, G.Lordan, J.Machado, R.D.MacKenzie Ross, R.V.McCabe, C.Moledina, S.Montani, D.Olschewski, H.Penkett, C.J.Pepke-Zaba, J.Price, L.Rhodes, C.J.Seeger, W.Soubrier, F.Southgate, L.Suntharalingam, J.Swift, A.J.Toshner, M.R.Noordegraaf, A.V.Wharton, J.Wild, J.Wort, S.J.Bogaard, H.J.Church, C.Coghlin, G.Condliffe, R.Eyries, M.Gall, H.Ghio, S.Girerd, B.Holden, S.Kiely, D.G.Kovacs, G.Lordan, J.Machado, R.D.MacKenzie Ross, R.V.McCabe, C.Moledina, S.Montani, D.Olschewski, H.Penkett, C.J.Pepke-Zaba, J.Price, L.Rhodes, C.J.Seeger, W.Soubrier, F.Suntharalingam, J.Swift, A.J.Toshner, M.R.Noordegraaf, A.V.Wharton, J.Wild, J.Wort, S.J.Gonzaga-Juaregui, C.
Source
In: Genome Medicine. (Genome Medicine, 01 December 2021, 13(1))
Subject
Language
English
ISSN
1756994X