Authors:
Bassi, MT
Bergen, AAB
Bitoun, P
Charles, SJ
Clementi, M
Gosselin, R
Hurst, J
Lewis, RA
Lorenz, B
Meitinger, T
Messiaen, L
Ramesar, RS
Ballabio, A
Schiaffino, MV
Citation: Mt. Bassi et al., Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America, HUM GENET, 108(1), 2001, pp. 51-54
Authors:
d'Addio, M
Pizzigoni, A
Bassi, MT
Baschirotto, C
Valetti, C
Incerti, B
Clementi, M
De Luca, M
Ballabio, A
Schiaffino, MV
Citation: M. D'Addio et al., Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1, HUM MOL GEN, 9(20), 2000, pp. 3011-3018
Authors:
Incerti, B
Cortese, K
Pizzigoni, A
Surace, EM
Varani, S
Coppola, M
Jeffery, G
Seeliger, M
Jaissle, G
Bennett, DC
Marigo, V
Schiaffino, MV
Tacchetti, C
Ballabio, A
Citation: B. Incerti et al., Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1, HUM MOL GEN, 9(19), 2000, pp. 2781-2788
Authors:
Schiaffino, MV
d'Addio, M
Alloni, A
Baschirotto, C
Valetti, C
Cortese, K
Puri, C
Bassi, MT
Colla, C
De Luca, M
Tacchetti, C
Ballabio, A
Citation: Mv. Schiaffino et al., Ocular albinism: evidence for a defect in an intracellular signal transduction system, NAT GENET, 23(1), 1999, pp. 108-112
Citation: Wn. Burns et al., Repeated transmission of X-linked ocular albinism type 1 by a carrier oocyte donor, FERT STERIL, 70(6), 1998, pp. 1169-1172