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http://hdl.handle.net/2183/37011

Cryptic splice-altering variants in MYBPC3 are a prevalent cause of hypertrophic cardiomyopathy

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URI: http://hdl.handle.net/2183/37011
DOI: 10.1161/CIRCGEN.120.002905

Publication date

2020-05-12

Authors

Lopes, Luis R.
Barbosa, Pedro
Quinn, Ellie
Merino, Ana
Jager, Joanna
Futema, Marta
Carmo-Fonseca, María
Montserrat, Lorenzo

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Lopes LR, Barbosa P, Torrado M, Quinn E, Merino A, Ochoa JP, Jager J, Futema M, Carmo-Fonseca M, Monserrat L, Syrris P, Elliott PM. Cryptic splice-altering variants in MYBPC3 are a prevalent cause of hypertrophic cardiomyopathy. Circ Genom Precis Med. 2020 Jun;13(3):e002905.

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Keywords

MYBPC3 Cardiomyopathy Hypertrophic Cryptic splice sites Genetics Introns

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https://doi.org/10.1161/circgen.120.002905

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Creative Commons Attribution-NonCommercial 4.0 International License (CC-BY-NC 4.0)

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Creative Commons Attribution-NonCommercial 4.0 International License (CC-BY-NC 4.0)

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