A 3-base pair insertional mutation in the choroideremia gene

Hum Mutat. 1998:Suppl 1:S38-9. doi: 10.1002/humu.1380110113.

Authors

N Nesslinger¹, S Horrocks, P N Ray, P Strasberg, I M MacDonald

Affiliation

¹ Ocular Genetics Laboratory, Department of Ophthalmology, University of Alberta, Edmonton, Canada.

PMID: 9452034
DOI: 10.1002/humu.1380110113

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Amino Acid Sequence
Base Sequence
Choroideremia / genetics*
Codon, Terminator / genetics
DNA / chemistry
DNA / genetics
DNA Mutational Analysis
Exons / genetics
Family Health
Female
Humans
Male
Mutagenesis, Insertional
Mutation
Polymorphism, Single-Stranded Conformational

Substances

Codon, Terminator
DNA