van den Hurk, J. A. J. M., van de Pol, D. J. R., Wissinger, B., van Driel, M. A., Hoefsloot, L. H., de Wijs, I. J., van den
Born, L. I., Heckenlively, J. R., Brunner, H. G., Zrenner, E., Ropers, H.-H., & Cremers, F. P. M. (2003).
Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a
cryptic exon. Human Genetics, 113(3), 268-275. doi:10.1007/s00439-003-0970-0.