PDE3A mutations cause autosomal dominant hypertension with brachydactyly
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Published:2015-05-11
Issue:6
Volume:47
Page:647-653
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ISSN:1061-4036
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Container-title:Nature Genetics
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language:en
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Short-container-title:Nat Genet
Author:
Maass Philipp G, Aydin Atakan, Luft Friedrich C, Schächterle 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, Mühl Astrid, Kann Martin, Schuster Herbert, Chitayat David, Bialer Martin G, Wienker Thomas F, Ott Jürg, Rittscher Katharina, Liehr Thomas, Jordan Jens, Plessis Ghislaine, Tank Jens, Mai Knut, Naraghi Ramin, Hodge Russell, Hopp Maxwell, Hattenbach Lars O, Busjahn AndreasORCID, Rauch Anita, Vandeput Fabrice, Gong Maolian, Rüschendorf Franz, Hübner Norbert, Haller Hermann, Mundlos Stefan, Bilginturan Nihat, Movsesian Matthew A, Klussmann Enno, Toka Okan, Bähring Sylvia
Publisher
Springer Science and Business Media LLC
Reference55 articles.
1. Hunter, D.J. & Reddy, K.S. Noncommunicable diseases. N. Engl. J. Med. 369, 1336–1343 (2013). 2. Schuster, H. et al. Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12. Nat. Genet. 13, 98–100 (1996). 3. Schuster, H. et al. A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly. Kidney Int. 53, 167–172 (1998). 4. Naraghi, R. et al. Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly. Stroke 28, 1749–1754 (1997). 5. Lifton, R.P. Genetic dissection of human blood pressure variation: common pathways from rare phenotypes. Harvey Lect. 100, 71–101 (2004).
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