Dominant optic atrophy in Denmark - report of 15 novel mutations in OPA1, using a strategy with a detection rate of 90%

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Investigation of the OPA1 mutation spectrum in autosomal dominant optic atrophy (ADOA) in Denmark.
OriginalsprogEngelsk
TidsskriftBMC Medical Genetics
Vol/bind13
Sider (fra-til)65
ISSN1471-2350
DOI
StatusUdgivet - aug. 2012

ID: 47684668