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Q36458923-44E19496-D0F7-4461-B1AB-F635745115D2
Q36458923-44E19496-D0F7-4461-B1AB-F635745115D2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36458923-44E19496-D0F7-4461-B1AB-F635745115D2
A novel splice site mutation of CDHR1 in a consanguineous Israeli Christian Arab family segregating autosomal recessive cone-rod dystrophy.
P2860
Q36458923-44E19496-D0F7-4461-B1AB-F635745115D2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36458923-44E19496-D0F7-4461-B1AB-F635745115D2
rank
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type
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Statement
wasDerivedFrom
9948ea902cbedf7efc1fb89f759d0eb2864fc05e
P2860
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II