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Q36341418-BF029EC0-DEF4-45CB-8827-8B431E02EC82
Q36341418-BF029EC0-DEF4-45CB-8827-8B431E02EC82
BestRank
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http://www.wikidata.org/entity/statement/Q36341418-BF029EC0-DEF4-45CB-8827-8B431E02EC82
Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing.
P2860
Q36341418-BF029EC0-DEF4-45CB-8827-8B431E02EC82
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36341418-BF029EC0-DEF4-45CB-8827-8B431E02EC82
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wasDerivedFrom
16940ff1ede31f1fec32586a639f39940727caa3
P2860
Domains of human U4atac snRNA required for U12-dependent splicing in vivo