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Q33681497-C86A62BF-A042-44B7-8430-D9B469712B5B
Q33681497-C86A62BF-A042-44B7-8430-D9B469712B5B
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http://www.wikidata.org/entity/statement/Q33681497-C86A62BF-A042-44B7-8430-D9B469712B5B
First report of OPA1 screening in Greek patients with autosomal dominant optic atrophy and identification of a previously undescribed OPA1 mutation.
P2860
Q33681497-C86A62BF-A042-44B7-8430-D9B469712B5B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33681497-C86A62BF-A042-44B7-8430-D9B469712B5B
rank
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Statement
wasDerivedFrom
8328936ec187cf1b62edee95334b108298e40f15
P2860
The prevalence and natural history of dominant optic atrophy due to OPA1 mutations.