Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications.

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Bibliographic Details
Title: Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications.
Authors: Mansoorshahi S; Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, TX, USA., Yetman AT; Children's Hospital and Medical Center, University of Nebraska, Omaha, NE, USA., Bissell MM; Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK., Kim YY; Division of Cardiovascular Medicine, The Hospital of the University of Pennsylvania, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA., Michelena HI; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA., De Backer J; Department of Cardiology and Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium., Mosquera LM; Department of Cardiology and Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium., Hui DS; Department of Cardiothoracic Surgery, University of Texas Health Science Center, San Antonio, TX, USA., Caffarelli A; Department of Cardiothoracic Surgery, Stanford University School of Medicine, Stanford, CA, USA., Andreassi MG; Consiglio Nazionale delle Richerche (CNR), Instituto di Fisiologia Clinica, Pisa, Italy., Foffa I; Consiglio Nazionale delle Richerche (CNR), Instituto di Fisiologia Clinica, Pisa, Italy., Guo D; Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, TX, USA., Citro R; Cardiothoracic and Vascular Department, University Hospital 'San Giovanni di Dio e Ruggi d'Aragona,' Salerno, Italy., De Marco M; Department of Medicine, Surgery and Dentistry Schola Medica Salernitana, University of Salerno, Baronissi, Italy., Tretter JT; Cleveland Clinic, Cleveland, OH, USA., Morris SA; Department of Pediatrics, Texas Children's Hospital and Baylor College of Medicine, Houston, TX, USA., Body SC; Department of Anesthesiology, Boston University School of Medicine, Boston, MA, USA., Chong JX; Department of Pediatrics, University of Washington, Seattle, WA, USA., Bamshad MJ; Department of Pediatrics, University of Washington, Seattle, WA, USA., Milewicz DM; Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, TX, USA., Prakash SK; Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, TX, USA. Electronic address: siddharth.k.prakash@uth.tmc.edu.
Corporate Authors: University of Washington Center for Rare Disease Research, BAVCon Investigators, EBAV Investigators
Source: American journal of human genetics [Am J Hum Genet] 2024 Oct 03; Vol. 111 (10), pp. 2219-2231. Date of Electronic Publication: 2024 Sep 02.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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