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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. [electronic resource] 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, Angel
- Brion, María
Producer: 20150512
In:
Clinica chimica acta; international journal of clinical chemistry vol. 437
Availability: No items available.
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