Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy

Autor: Restrepo-Cordoba M, Wahbi K, Florian A, Jimenez-Jaimez J, Politano L, Arad M, Climent-Paya V, Garcia-Alvarez A, Hansen R, Larranaga-Moreira J, Kubanek M, Lopes L, Ros A, Jurcut R, Rasmussen T, Ruiz-Guerrero L, Pribe-Wolferts R, Palomino-Doza J, Bilinska Z, Rodriguez-Palomares J, Van Loon R, Elorz M, Quarta G, Inarritu M, Verdonschot J, Stojkovic T, Shomanova Z, Bermudez-Jimenez F, Palladino A, Freimark D, Garcia-Alvarez M, Jorda P, Dominguez F, Ochoa J, Girolami F, Brugada R, Meder B, Barriales-Villa R, Mogensen J, Laforet P, Yilmaz A, Elliott P, Garcia-Pavia P, European Genetic Cardiomyopathies

Publikováno v: EUROPEAN JOURNAL OF HEART FAILURE
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
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Aims Dilated cardiomyopathy (DCM) associated with dystrophin gene (DMD) mutations in individuals with mild or absent skeletal myopathy is often indistinguishable from other DCM forms. We sought to describe the phenotype and prognosis of DMD associate

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::76f7a64b142e26b6af4c81ed3659725b
https://fundanet.isabial.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=7535

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