Mapping of the choroideremia-like (CHML) gene at 1q42-qter and mutation analysis in patients with Usher syndrome type II.

Autor: von Bokhoven H; Department of Human Genetics, University Hospital Nijmegen, The Netherlands., von Genderen C, Molloy CM, van de Pol DJ, Cremers CW, von Aarem A, Schwartz M, Rosenberg T, Geurts van Kessel AH, Ropers HH, et. al.

Publikováno v: Genomics [Genomics] 1994 Jan 15; Vol. 19 (2), pp. 385-7.