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Q34789718-23D0E7DF-0E9F-4842-9933-A03D75352C51
Q34789718-23D0E7DF-0E9F-4842-9933-A03D75352C51
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Statement
http://www.wikidata.org/entity/statement/Q34789718-23D0E7DF-0E9F-4842-9933-A03D75352C51
Targeted exon sequencing in Usher syndrome type I
P2860
Q34789718-23D0E7DF-0E9F-4842-9933-A03D75352C51
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34789718-23D0E7DF-0E9F-4842-9933-A03D75352C51
rank
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wasDerivedFrom
6eeca880f3f31d6a2b3ec016a02e16464fa9d7df
P2860
NMNAT1 mutations cause Leber congenital amaurosis