Pubblicazioni

Physics of selective conduction and point mutation in biological ion channels

2021 - PHYSICAL REVIEW LETTERS
Gibby, W. A. T.; Barabash, M. L.; Guardiani, C.; Luchinsky, D. G.; Mcclintock, P. V. E.

Hereditary neuropathy with liability to pressure palsy (HNPP): Report of a family with a new point mutation in PMP22 gene

2017 - THE ITALIAN JOURNAL OF PEDIATRICS
Fusco, C.; Spagnoli, C.; Salerno, G. G.; Pavlidis, E.; Frattini, D.; Pisani, F.

Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylation

2015 - THROMBOSIS RESEARCH
Asselta, Rosanna; Robusto, Michela; Platé, Manuela; Santoro, Cristina; Peyvandi, Flora; Duga, Stefano

© Università degli Studi di Roma "La Sapienza" - Piazzale Aldo Moro 5, 00185 Roma