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Q34689838-C184B63D-B984-4085-9D8D-46C212024C1F
Q34689838-C184B63D-B984-4085-9D8D-46C212024C1F
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http://www.wikidata.org/entity/statement/Q34689838-C184B63D-B984-4085-9D8D-46C212024C1F
Synaptic determinants of rett syndrome.
P2860
Q34689838-C184B63D-B984-4085-9D8D-46C212024C1F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34689838-C184B63D-B984-4085-9D8D-46C212024C1F
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wasDerivedFrom
0db443958e02739cc537dcc05375a2322b647bb7
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression