Piccolo, P., Sabatino, V., Mithbaokar, P., Polishchuk, E., Hicks, J., Polishchuk, R., . . . Brunetti‐Pierri, N. (2019). Skin fibroblasts of patients with geleophysic dysplasia due to FBN1 mutations have lysosomal inclusions and losartan improves their microfibril deposition defect. Mol Genet Genomic Med.
Citación estilo ChicagoPiccolo, Pasquale, Valeria Sabatino, Pratibha Mithbaokar, Elena Polishchuk, John Hicks, Roman Polishchuk, Carlos A. Bacino, y Nicola Brunetti‐Pierri. "Skin Fibroblasts of Patients With Geleophysic Dysplasia Due to FBN1 Mutations Have Lysosomal Inclusions and Losartan Improves Their Microfibril Deposition Defect." Mol Genet Genomic Med 2019.
Cita MLAPiccolo, Pasquale, et al. "Skin Fibroblasts of Patients With Geleophysic Dysplasia Due to FBN1 Mutations Have Lysosomal Inclusions and Losartan Improves Their Microfibril Deposition Defect." Mol Genet Genomic Med 2019.