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Detalhes Referência

Tipo
Artigos em Revista

Tipo de Documento
Artigo Completo

Título
Cryptic Splice-Altering Variants in MYBPC3 Are a Prevalent Cause of Hypertrophic Cardiomyopathy

Participantes na publicação
Luis R. Lopes (Author)
Pedro Barbosa (Author)
LASIGE
Mario Torrado (Author)
Ellie Quinn (Author)
Ana Merino (Author)
Juan Pablo Ochoa (Author)
Joanna Jager (Author)
Marta Futema (Author)
Maria Carmo-Fonseca (Author)
Lorenzo Monserrat (Author)
Petros Syrris (Author)
Perry M. Elliott (Author)

Data de Publicação
2020-06

Suporte
Circulation: Genomic and Precision Medicine

Identificadores da Publicação
ISSN - 2574-8300

Editora
Ovid Technologies (Wolters Kluwer Health)

Volume
13
Fascículo
3

Identificadores do Documento
DOI - https://doi.org/10.1161/circgen.120.002905
URL - http://dx.doi.org/10.1161/circgen.120.002905


Exportar referência

APA
Luis R. Lopes, Pedro Barbosa, Mario Torrado, Ellie Quinn, Ana Merino, Juan Pablo Ochoa, Joanna Jager, Marta Futema, Maria Carmo-Fonseca, Lorenzo Monserrat, Petros Syrris, Perry M. Elliott, (2020). Cryptic Splice-Altering Variants in MYBPC3 Are a Prevalent Cause of Hypertrophic Cardiomyopathy. Circulation: Genomic and Precision Medicine, 13, ISSN 2574-8300. eISSN . http://dx.doi.org/10.1161/circgen.120.002905

IEEE
Luis R. Lopes, Pedro Barbosa, Mario Torrado, Ellie Quinn, Ana Merino, Juan Pablo Ochoa, Joanna Jager, Marta Futema, Maria Carmo-Fonseca, Lorenzo Monserrat, Petros Syrris, Perry M. Elliott, "Cryptic Splice-Altering Variants in MYBPC3 Are a Prevalent Cause of Hypertrophic Cardiomyopathy" in Circulation: Genomic and Precision Medicine, vol. 13, 2020. 10.1161/circgen.120.002905

BIBTEX
@article{58966, author = {Luis R. Lopes and Pedro Barbosa and Mario Torrado and Ellie Quinn and Ana Merino and Juan Pablo Ochoa and Joanna Jager and Marta Futema and Maria Carmo-Fonseca and Lorenzo Monserrat and Petros Syrris and Perry M. Elliott}, title = {Cryptic Splice-Altering Variants in MYBPC3 Are a Prevalent Cause of Hypertrophic Cardiomyopathy}, journal = {Circulation: Genomic and Precision Medicine}, year = 2020, volume = 13 }