Article Versions Notes

Di Giosaffatte N, Ferraris A, Gaudioso F, Lodato V, Savino E, Celletti C, Camerota F, Bargiacchi S, Laino L, Majore S, et al. Congenital Defects in a Patient Carrying a Novel Homozygous AEBP1 Variant: Further Expansion of the Phenotypic Spectrum of Ehlers–Danlos Syndrome Classical-like Type 2? Genes. 2022; 13(12):2358. https://doi.org/10.3390/genes13122358

Di Giosaffatte, Niccolò, Alessandro Ferraris, Federica Gaudioso, Valentina Lodato, Emanuele Savino, Claudia Celletti, Filippo Camerota, Simone Bargiacchi, Luigi Laino, Silvia Majore, and et al. 2022. "Congenital Defects in a Patient Carrying a Novel Homozygous AEBP1 Variant: Further Expansion of the Phenotypic Spectrum of Ehlers–Danlos Syndrome Classical-like Type 2?" Genes 13, no. 12: 2358. https://doi.org/10.3390/genes13122358

Di Giosaffatte, N., Ferraris, A., Gaudioso, F., Lodato, V., Savino, E., Celletti, C., Camerota, F., Bargiacchi, S., Laino, L., Majore, S., Bottillo, I., & Grammatico, P. (2022). Congenital Defects in a Patient Carrying a Novel Homozygous AEBP1 Variant: Further Expansion of the Phenotypic Spectrum of Ehlers–Danlos Syndrome Classical-like Type 2? Genes, 13(12), 2358. https://doi.org/10.3390/genes13122358