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Q34493173-21234B29-F932-4813-8DCE-E89AFC59A810
Q34493173-21234B29-F932-4813-8DCE-E89AFC59A810
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34493173-21234B29-F932-4813-8DCE-E89AFC59A810
Novel genetic causes for cerebral visual impairment
P2860
Q34493173-21234B29-F932-4813-8DCE-E89AFC59A810
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34493173-21234B29-F932-4813-8DCE-E89AFC59A810
rank
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type
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wasDerivedFrom
7d0015221d8bdc5c61b89e3938d619024079f64e
P2860
NR2F1 mutations cause optic atrophy with intellectual disability.