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