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Q36663018-63F46A1A-779C-471C-9830-0FB57B910B9C
Q36663018-63F46A1A-779C-471C-9830-0FB57B910B9C
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http://www.wikidata.org/entity/statement/Q36663018-63F46A1A-779C-471C-9830-0FB57B910B9C
X-linked mental retardation and epigenetics.
P2860
Q36663018-63F46A1A-779C-471C-9830-0FB57B910B9C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36663018-63F46A1A-779C-471C-9830-0FB57B910B9C
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wasDerivedFrom
f23f8dc0c8fabde7e2e91b07d6437786352357b5
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression