Authors:
Bolz, H
von Brederlow, B
Ramirez, A
Bryda, EC
Kutsche, K
Nothwang, HG
Seeliger, M
Cabrera, MDS
Vila, MC
Molina, OP
Gal, A
Kubisch, C
Citation: H. Bolz et al., Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D, NAT GENET, 27(1), 2001, pp. 108-112
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:
Biel, M
Seeliger, M
Pfeifer, A
Kohler, K
Gerstner, A
Ludwig, A
Jaissle, G
Fauser, S
Zrenner, E
Hofmann, F
Citation: M. Biel et al., Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3, P NAS US, 96(13), 1999, pp. 7553-7557