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Q30368414-711793DC-DE68-432C-8106-A730F60DA0C1
Q30368414-711793DC-DE68-432C-8106-A730F60DA0C1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30368414-711793DC-DE68-432C-8106-A730F60DA0C1
A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family
P2860
Q30368414-711793DC-DE68-432C-8106-A730F60DA0C1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30368414-711793DC-DE68-432C-8106-A730F60DA0C1
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wasDerivedFrom
a60300fb927534f3763f80a1f9b9a83531099aac
P2860
Molecular diagnosis of putative Stargardt disease by capture next generation sequencing