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 - 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
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