Browse by Person
 | Up a level |
Number of items: 2.
Ronzoni, R. and Berardelli, R. and Medicina, D. and Sitia, R. and Gooptu, Bibek and Fra, A.M. (2016) Aberrant disulphide bonding contributes to the ER retention of alpha1-antitrypsin deficiency variants. Human Molecular Genetics 25 (4), pp. 642-650. ISSN 0964-6906.
Gasset, M. and Fra, A.M. and Gooptu, Bibek and Ferrarotti, I. and Miranda, E. and Scabini, R. and Ronzoni, R. and Benini, F. and Corda, L. and Medicina, D. and Luisetti, M. and Schiaffonati, L. (2012) Three new Alpha1-Antitrypsin deficiency variants help to define a C-Terminal region regulating conformational change and polymerization. PLoS One 7 (6), ISSN 1932-6203.