eP142 - Barth syndrome caused by a novel TAZ deletion through an alu element-mediated mechanism: a case report.

Autor: Vossaert, Liesbeth (AUTHOR), Lattier, John (AUTHOR), Zhu, Wenmiao (AUTHOR), Dang, Anh (AUTHOR), Schroeder, Audrey (AUTHOR), Fong, Chin-To (AUTHOR), Dai, Hongzheng (AUTHOR)
Zdroj: Molecular Genetics & Metabolism. 2021 Supplement 1, Vol. 132, pS93-S95. 3p.
Databáze: Academic Search Ultimate