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) |
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Zdroj: | Molecular Genetics & Metabolism. 2021 Supplement 1, Vol. 132, pS93-S95. 3p. |
Databáze: | Academic Search Ultimate |
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