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Q33624742-D93C85A6-07D8-4439-884A-C5D3A26DD535
Q33624742-D93C85A6-07D8-4439-884A-C5D3A26DD535
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33624742-D93C85A6-07D8-4439-884A-C5D3A26DD535
XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients.
P2860
Q33624742-D93C85A6-07D8-4439-884A-C5D3A26DD535
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33624742-D93C85A6-07D8-4439-884A-C5D3A26DD535
rank
NormalRank
type
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wasDerivedFrom
4df58fa8b4db05280b4eece74ddf1bc6c34b8a63
P2860
Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship