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Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy? by Gehmlich, K, Asimaki, A, Cahill, T, Ehler, E, Syrris, P, Zachara, E, Re, F, Avella, A, Monserrat, L, Saffitz, J, McKenna, W
Published 2010Journal article -
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Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations by Chundru, VK, Zhang, Z, Walter, K, Lindsay, SJ, Danecek, P, Eberhardt, RY, Gardner, EJ, Malawsky, DS, Wigdor, EM, Torene, R, Retterer, K, Wright, CF, Ólafsdóttir, H, Guillen Sacoto, MJ, Ayaz, A, Akbeyaz, IH, Türkdoğan, D, Al Balushi, AI, Bertoli-Avella, A, Bauer, P, Szenker-Ravi, E, Reversade, B, McWalter, K, Sheridan, E
Published 2024Journal article