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Q35944038-28B648DC-D606-4B19-937E-913D0C37B820
Q35944038-28B648DC-D606-4B19-937E-913D0C37B820
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http://www.wikidata.org/entity/statement/Q35944038-28B648DC-D606-4B19-937E-913D0C37B820
Molecular genetic basis of primary inherited optic neuropathies.
P2860
Q35944038-28B648DC-D606-4B19-937E-913D0C37B820
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35944038-28B648DC-D606-4B19-937E-913D0C37B820
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wasDerivedFrom
b9734359acbcd47a43c6058267bc99a1c68b25e0
P2860
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