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Q27000489-DBD5C1FF-E79E-4261-8D5F-8C37D6A97370
Q27000489-DBD5C1FF-E79E-4261-8D5F-8C37D6A97370
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27000489-DBD5C1FF-E79E-4261-8D5F-8C37D6A97370
Human Mendelian diseases related to abnormalities of the RNA exosome or its cofactors
P2860
Q27000489-DBD5C1FF-E79E-4261-8D5F-8C37D6A97370
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27000489-DBD5C1FF-E79E-4261-8D5F-8C37D6A97370
rank
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wasDerivedFrom
91979307b8871348ba6a5e77704c09f4d49f17c4
P2860
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3.