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2
Q50535243-59695CC4-DFEF-4DE3-8FD3-5BC944680179
Q50535243-59695CC4-DFEF-4DE3-8FD3-5BC944680179
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http://www.wikidata.org/entity/statement/Q50535243-59695CC4-DFEF-4DE3-8FD3-5BC944680179
C8orf37 is mutated in Bardet-Biedl syndrome and constitutes a locus allelic to non-syndromic retinal dystrophies.
P2860
Q50535243-59695CC4-DFEF-4DE3-8FD3-5BC944680179
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50535243-59695CC4-DFEF-4DE3-8FD3-5BC944680179
rank
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type
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wasDerivedFrom
0f3ec65b3df47556ecac54723d851809cf5cf47e
P2860
Whole exome sequencing reveals GUCY2D as a major gene associated with cone and cone-rod dystrophy in Israel.