A recessive truncating variant in thrombospondin ‐1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous family

American Journal of Medical Genetics Part A, EarlyView.

Source: American Journal of Medical Genetics Part A - July 28, 2018 Category: Genetics & Stem Cells Authors: Hanadi A. Abdelrahman , Aisha Al ‐Shamsi , Anne John , Jozef Hertecant , Ali Lootah , Bassam R. Ali , Lihadh Al‐Gazali Source Type: research