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Q34326032-EFF23164-5F78-433E-AE90-65C992F4218A
Q34326032-EFF23164-5F78-433E-AE90-65C992F4218A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34326032-EFF23164-5F78-433E-AE90-65C992F4218A
Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy.
P2860
Q34326032-EFF23164-5F78-433E-AE90-65C992F4218A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34326032-EFF23164-5F78-433E-AE90-65C992F4218A
rank
NormalRank
type
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Statement
wasDerivedFrom
e3a25dce704a54c68f24663ac55f2aed685e1879
P2860
Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome.