1.
Callea M, Willoughby CE, Camarata-Scalisi F, Giovannoni I, Vinciguerra A, Yavuz I, Di Stazio M, Di Iorio E, Clarich G, Benettoni A, Galeotti A, Bellacchio E. A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype. Invest Clín [Internet]. 16 de marzo de 2017 [citado 5 de abril de 2025];58(1). Disponible en: https://produccioncientificaluz.org./index.php/investigacion/article/view/29043