PDE3A mutations cause autosomal dominant hypertension with brachydactyly

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PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Author: Maass, Philipp G.; Aydin, Atakan; Luft, Friedrich C.; Schaechterle, Carolin; Weise, Anja; Stricker, Sigmar; Lindschau, Carsten; Vaegler, Martin; Qadri, Fatimunnisa; Toka, Hakan R.; Schulz, Herbert; Krawitz, Peter M.; Parkhomchuk, Dmitri; Hecht, Jochen; Hollfinger, Irene; Wefeld-Neuenfeld, Yvette; Bartels-Klein, Eireen; Muehl, Astrid; Kann, Martin; Schuster, Herbert; Chitayat, David; Bialer, Martin G.; Wienker, Thomas F.; Ott, Juerg; Rittscher, Katharina; Liehr, Thomas; Jordan, Jens; Plessis, Ghislaine; Tank, Jens; Mai, Knut; Naraghi, Ramin; Hodge, Russell; Hopp, Maxwell; Hattenbach, Lars O.; Busjahn, Andreas; Rauch, Anita; Vandeput, Fabrice; Gong, Maolian; Rueschendorf, Franz; Huebner, Norbert; Haller, Hermann; Mundlos, Stefan; Bilginturan, Nihat; Movsesian, Matthew A.; Klussmann, Enno; Toka, Okan; Baehring, Sylvia
Tübinger Autor(en):
Vaegler, Martin
Published in: Nature Genetics (2015), Bd. 47, H. 6, S. 647-653
Verlagsangabe: Nature Publishing Group
Language: English
Full text: http://dx.doi.org/10.1038/ng.3302
ISSN: 1061-4036
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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