Identification of mutations in Danish choroideremia families.

Abstract

We have searched for mutations in the choroideremia gene (CHM) in patients from 12 Danish families in which CHM is segregating. Employing polymerase chain reaction (PCR), single strand conformation polymorphism (SSCP) analysis, and direct DNA sequencing, different mutations have been identified in 6 patients. All the mutations will interfere with the correct translation of the mRNA predicting a truncated protein or no gene product at all.

Cite this paper

@article{Schwartz1993IdentificationOM, title={Identification of mutations in Danish choroideremia families.}, author={Myron Eliot Schwartz and Thomas Rosenberg and Jos{\'e} A J M van den Hurk and Dorien J R van De Pol and Frans P. M. Cremers}, journal={Human mutation}, year={1993}, volume={2 1}, pages={43-7} }