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Q34187242-608110B9-2342-42BE-A9A7-F9F124D1E99E
Q34187242-608110B9-2342-42BE-A9A7-F9F124D1E99E
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Statement
http://www.wikidata.org/entity/statement/Q34187242-608110B9-2342-42BE-A9A7-F9F124D1E99E
Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL.
P2860
Q34187242-608110B9-2342-42BE-A9A7-F9F124D1E99E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34187242-608110B9-2342-42BE-A9A7-F9F124D1E99E
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wasDerivedFrom
d0e4e58b1fafad79e8d435fea6a73d76000c6caf
P2860
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.