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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 09-10-2017
Symbol MRX95
Location Xq21.1
Name mental retardation, X-linked 95
Corresponding gene MAGT1
Main clinical features
  • nonsyndromic X-linked mental retardation, severe mental retardation
  • patients with limited conversation, however, neither learned to read or write
  • Genetic determination sex linked
    Function/system disorder mental retardation
    Type disease
    Remark(s)