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Onore ME, Caiazza M, Farina A, Scarano G, Budillon A, Borrelli RN, Limongelli G, Nigro V, Piluso G. A Novel Homozygous Loss-of-Function Variant in SPRED2 Causes Autosomal Recessive Noonan-like Syndrome. Genes. 2024; 15(1):32. https://doi.org/10.3390/genes15010032

Onore, Maria Elena, Martina Caiazza, Antonella Farina, Gioacchino Scarano, Alberto Budillon, Rossella Nicoletta Borrelli, Giuseppe Limongelli, Vincenzo Nigro, and Giulio Piluso. 2024. "A Novel Homozygous Loss-of-Function Variant in SPRED2 Causes Autosomal Recessive Noonan-like Syndrome" Genes 15, no. 1: 32. https://doi.org/10.3390/genes15010032

Onore, M. E., Caiazza, M., Farina, A., Scarano, G., Budillon, A., Borrelli, R. N., Limongelli, G., Nigro, V., & Piluso, G. (2024). A Novel Homozygous Loss-of-Function Variant in SPRED2 Causes Autosomal Recessive Noonan-like Syndrome. Genes, 15(1), 32. https://doi.org/10.3390/genes15010032