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Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome
Warejko, Jillian K., Schueler, Markus, Vivante, Asaf, Tan, Weizhen, Daga, Ankana, Lawson, Jennifer A., Braun, Daniela A., Shril, Shirlee, Amann, Kassaundra, Somers, Michael J.G., Rodig, Nancy M., BaumLanguage:
english
Journal:
Hypertension
DOI:
10.1161/HYPERTENSIONAHA.117.10296
Date:
February, 2018
File:
PDF, 2.43 MB
english, 2018