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Q28363963-473DDECD-246A-48D7-8374-9A103F7EEFFC
Q28363963-473DDECD-246A-48D7-8374-9A103F7EEFFC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28363963-473DDECD-246A-48D7-8374-9A103F7EEFFC
Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene
P2860
Q28363963-473DDECD-246A-48D7-8374-9A103F7EEFFC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28363963-473DDECD-246A-48D7-8374-9A103F7EEFFC
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Statement
wasDerivedFrom
d6c9d89707947a0de50d9e9cd8f779ffb3290f94
P2860
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.