Authors:
Schwahn, U
Paland, N
Techritz, S
Lenzner, S
Berger, W
Citation: U. Schwahn et al., Mutations in the X-linked RP2 gene cause intracellular misrouting and lossof the protein, HUM MOL GEN, 10(11), 2001, pp. 1177-1183
Authors:
Brunner, B
Todt, T
Lenzner, S
Stout, K
Schulz, U
Ropers, HH
Kalscheuer, VM
Citation: B. Brunner et al., Genomic structure and comparative analysis of nine Fugu genes: Conservation of synteny with human chromosome Xp22.2-p22.1, GENOME RES, 9(5), 1999, pp. 437-448
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