Dominant optic atrophy in Denmark - report of 15 novel mutations in OPA1, using a strategy with a detection rate of 90%
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Investigation of the OPA1 mutation spectrum in autosomal dominant optic atrophy (ADOA) in Denmark.
Originalsprog | Engelsk |
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Tidsskrift | BMC Medical Genetics |
Vol/bind | 13 |
Sider (fra-til) | 65 |
ISSN | 1471-2350 |
DOI | |
Status | Udgivet - aug. 2012 |
ID: 47684668