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Q24630545-AA41BF4B-6F66-4B07-88BA-DB6146ED9628
Q24630545-AA41BF4B-6F66-4B07-88BA-DB6146ED9628
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24630545-AA41BF4B-6F66-4B07-88BA-DB6146ED9628
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
P2860
Q24630545-AA41BF4B-6F66-4B07-88BA-DB6146ED9628
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24630545-AA41BF4B-6F66-4B07-88BA-DB6146ED9628
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wasDerivedFrom
b26fccc8857b85a0e7b0653ab776dd9b40e50857
P2860
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2