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
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| Description | scientific article published on 28 July 2018 |
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author: Lihadh Al-Gazali |
| Publication date | July 28, 2018 |
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