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Whole Exome Sequencing,Familial Genomic Triangulation,and Systems Biology Converge to Identify a Novel Nonsense Mutation in TAB2‐encoded TGF‐beta Activated Kinase 1 in a Child with Polyvalvular Syndrome
Authors:Jaeger P. Ackerman BA  John A. Smestad BS  David J. Tester BS  Muhammad Y. Qureshi MBBS  Beau A. Crabb MS  CGC  Nancy J. Mendelsohn MD  Michael J. Ackerman MD  PhD
Affiliation:1. Departments of Cardiovascular Diseases (Division of Heart Rhythm Services), Pediatrics (Division of Pediatric Cardiology), and Molecular Pharmacology & Experimental Therapeutics (Windland Smith Rice Sudden Death Genomics Laboratory), Mayo Clinic, Rochester, Minn, USA;2. Mayo Clinic Medical Scientist Training Program, Rochester, Minn, USA;3. Department of Medical Genetics, Children's Hospital and Clinics of Minnesota, Minneapolis, Minn, USA
Abstract:
Keywords:Polyvalvular Syndrome  Whole Exome Sequencing  TAB2
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