Authors:
Pusch, CM
Zeitz, C
Brandau, O
Pesch, K
Achatz, H
Feil, S
Scharfe, C
Maurer, J
Jacobi, FK
Pinckers, A
Andreasson, S
Hardcastle, A
Wissinger, B
Berger, W
Meindl, A
Citation: Cm. Pusch et al., The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein, NAT GENET, 26(3), 2000, pp. 324-327
Authors:
Kirschner, R
Rosenberg, T
Schultz-Heienbrok, R
Lenzner, S
Feil, S
Roepman, R
Cremers, FPM
Ropers, HH
Berger, W
Citation: R. Kirschner et al., RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa, HUM MOL GEN, 8(8), 1999, pp. 1571-1578