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Q38148981-A763F501-EB62-46B6-AF5B-BCEA9F33615E
Q38148981-A763F501-EB62-46B6-AF5B-BCEA9F33615E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38148981-A763F501-EB62-46B6-AF5B-BCEA9F33615E
E6AP in the brain: one protein, dual function, multiple diseases.
P2860
Q38148981-A763F501-EB62-46B6-AF5B-BCEA9F33615E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38148981-A763F501-EB62-46B6-AF5B-BCEA9F33615E
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wasDerivedFrom
20e4dc613922601efec1f5fac43ba133969d0d79
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression