Chiarelli, N., Carini, G., Zoppi, N., Ritelli, M., & Colombi, M. (2018). Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome. PLoS One.

Chiarelli, Nicola, Giulia Carini, Nicoletta Zoppi, Marco Ritelli, a Marina Colombi. "Transcriptome Analysis of Skin Fibroblasts With Dominant Negative COL3A1 Mutations Provides Molecular Insights Into the Etiopathology of Vascular Ehlers-Danlos Syndrome." PLoS One 2018.

Chiarelli, Nicola, et al. "Transcriptome Analysis of Skin Fibroblasts With Dominant Negative COL3A1 Mutations Provides Molecular Insights Into the Etiopathology of Vascular Ehlers-Danlos Syndrome." PLoS One 2018.