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Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

✍ Scribed by Gago-Díaz, Marina; Blanco-Verea, Alejandro; Teixidó-Turà, Gisela; Valenzuela, Irene; Del Campo, Miguel; Borregan, Mar; Sobrino, Beatriz; Amigo, Jorge; García-Dorado, David; Evangelista, Artur; Carracedo, Ángel; Brion, María

Book ID: 125817626
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 779 KB
Volume: 437
Category: Article
ISSN: 0009-8981
DOI: 10.1016/j.cca.2014.07.016

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