Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome
Jillian K. Warejko,M. Schueler,25 Authors,F. Hildebrandt
2018 · DOI: 10.1161/HYPERTENSIONAHA.117.10296
HYPERTENSION · 23 Citations
TLDR
Establishing an etiologic diagnosis may reveal genotype/phenotype correlations for MAS in the future and should, therefore, be performed routinely in MAS.