| Literature DB >> 7465492 |
K M Cheng, R N Shoffner, K N Gelatt, G G Gum, J S Otis, J J Bitgood.
Abstract
A type of blindness due to lack of rods and cones in the retina was found to be controlled by a single autosomal recessive gene, rc. The mutation was first identified in the second generation descendants of a male carrying an ethyl methanesulfonate (EMS) induced chromosome translocation involving one arm of the Z sex chromosome and the long (q) arm of chromosome 3. A linkage test between the locus causing the blindness and the translocation break-point on chromosome 3 was not significant. There is no proof that the mutation was EMS induced.Entities:
Mesh:
Year: 1980 PMID: 7465492 DOI: 10.3382/ps.0592179
Source DB: PubMed Journal: Poult Sci ISSN: 0032-5791 Impact factor: 3.352