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Q36957262-0F322BB7-84B7-449E-B506-99A768CDE450
Q36957262-0F322BB7-84B7-449E-B506-99A768CDE450
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http://www.wikidata.org/entity/statement/Q36957262-0F322BB7-84B7-449E-B506-99A768CDE450
Loss of RPGR glutamylation underlies the pathogenic mechanism of retinal dystrophy caused by TTLL5 mutations
P2860
Q36957262-0F322BB7-84B7-449E-B506-99A768CDE450
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36957262-0F322BB7-84B7-449E-B506-99A768CDE450
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wasDerivedFrom
2a0248582d3e62f2c4d50cc7737a1b7d9e339a62
P2860
Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophy