Whole gene sequencing identifies deep-intronic variants with potential functional impact in patients with hypertrophic cardiomyopathy.
Autor: | Mendes de Almeida, Rita1, Tavares, Joana1, Martins, Sandra1, Carvalho, Teresa1, Enguita, Francisco J.1, Brito, Dulce2,3, Carmo-Fonseca, Maria1 carmo.fonseca@medicina.ulisboa.pt, Lopes, Luís Rocha3,4 lrlopes@medicina.ulisboa.pt |
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Zdroj: | PLoS ONE. 8/10/2017, Vol. 12 Issue 8, p1-19. 19p. |
Databáze: | Academic Search Ultimate |
Externí odkaz: |