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Q47879364-4CEFBF55-0916-47BC-9949-531C0FDECEE0
Q47879364-4CEFBF55-0916-47BC-9949-531C0FDECEE0
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http://www.wikidata.org/entity/statement/Q47879364-4CEFBF55-0916-47BC-9949-531C0FDECEE0
GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.
P2860
Q47879364-4CEFBF55-0916-47BC-9949-531C0FDECEE0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47879364-4CEFBF55-0916-47BC-9949-531C0FDECEE0
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wasDerivedFrom
1b6ada30a04e732600af1d2dd235c50f5b15956b
P2860
Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2.