A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect
- 1 November 2001
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 109 (5) , 498-502
- https://doi.org/10.1007/s004390100600
Abstract
No abstract availableKeywords
This publication has 0 references indexed in Scilit: