Whole-exome sequencing identifies a de novo PDE3A variant causing autosomal dominant hypertension with brachydactyly type E syndrome: a case report.
Xianqing LiZongzhe LiPeng ChenYan WangDao Wen WangDao Wu WangPublished in: BMC medical genetics (2020)
We present a report linking a de novo PDE3A variant to autosomal dominant hypertension with brachydactyly type E syndrome.