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Q36467228-E0A072ED-A9E8-4BCD-920E-B7A2171E9EC5
Q36467228-E0A072ED-A9E8-4BCD-920E-B7A2171E9EC5
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Statement
http://www.wikidata.org/entity/statement/Q36467228-E0A072ED-A9E8-4BCD-920E-B7A2171E9EC5
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease
P2860
Q36467228-E0A072ED-A9E8-4BCD-920E-B7A2171E9EC5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36467228-E0A072ED-A9E8-4BCD-920E-B7A2171E9EC5
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wasDerivedFrom
45a1d721f7b41ac3dfaeca40f10eac6744def603
P2860
RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa