Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.
- Resource Type
- journal article
- Authors
- Warejkov, Jillian K.; Schueler, Markus; Vivante, Asaf; Weizhen Tan; Daga, Ankana; Lawson, Jennifer A.; Braun, Daniela A.; Shril, Shirlee; Amann, Kassaundra; Somers, Michael J. G.; Rodig, Nancy M.; Baum, Michelle A.; Daouk, Ghaleb; Traum, Avram Z.; Heung Bae Kim; Vakili, Khashayar; Porras, Diego; Lock, James; Rivkin, Michael J.; Chaudry, Gulraiz
- Source
- Hypertension (0194911X); Apr2018, Vol. 71 Issue 4, p691-699, 9p, 1 Diagram, 3 Charts, 1 Graph
- Subject
- Language
- ISSN
- 0194911X