Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.

doi:10.1016/0888-7543(92)90394-8

Back to search

Article

Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.

Genomics - 1 Feb 1992

Bech-Hansen N T, Moore B J, Pearce W G

Abstract excerpt

A recombinant chromosome in a male affected with X-linked congenital stationary night blindness (CSNB1) provides new information on the location of the CSNB1 locus. A four-generation family with five males affected with X-linked CSNB was analyzed with five polymorphic markers for four X-chromosom...

Topics

Alleles
Chromosome Mapping
Female
Genetic Linkage
Haplotypes
Humans
Male
Night Blindness
Pedigree
X Chromosome

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.