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Q36957262-675EAC33-7F36-4707-8B59-5EDE95BCEE85
Q36957262-675EAC33-7F36-4707-8B59-5EDE95BCEE85
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Statement
http://www.wikidata.org/entity/statement/Q36957262-675EAC33-7F36-4707-8B59-5EDE95BCEE85
Loss of RPGR glutamylation underlies the pathogenic mechanism of retinal dystrophy caused by TTLL5 mutations
P2860
Q36957262-675EAC33-7F36-4707-8B59-5EDE95BCEE85
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36957262-675EAC33-7F36-4707-8B59-5EDE95BCEE85
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wasDerivedFrom
2a0248582d3e62f2c4d50cc7737a1b7d9e339a62
P2860
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease