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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 09-10-2017
Symbol MRX89
Location Xp11.3
Name mental retardation, 89
Corresponding gene ZNF41
Main clinical features nonsyndromic X-linked mental retardation, with language retardation, avoided social contact
Genetic determination sex linked
Function/system disorder mental retardation
Type disease
Remark(s)