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
Titel:
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
Auteur:
Thiselton, Dawn L. Alexander, Christiane Morris, Alex Brooks, Simon Rosenberg, Thomas Eiberg, Hans Kjer, Birgit Kjer, Poul Bhattacharya, Shomi S. Votruba, Marcela