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Q36531483-85A9FD51-A4D9-427D-A7D2-C51A46930C12
Q36531483-85A9FD51-A4D9-427D-A7D2-C51A46930C12
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36531483-85A9FD51-A4D9-427D-A7D2-C51A46930C12
Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers.
P2860
Q36531483-85A9FD51-A4D9-427D-A7D2-C51A46930C12
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36531483-85A9FD51-A4D9-427D-A7D2-C51A46930C12
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wasDerivedFrom
7c64698a8139fdd4d5feb5788a23800a9148e148
P2860
ABCA4 and ROM1: implications for modification of the PRPH2-associated macular dystrophy phenotype.