(Q50349635)

English

autosomal dominant non-syndromic intellectual disability 31

An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of PURA on chromosome 5q31.3.

  • MRD31
  • autosomal dominant mental retardation 31
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 31
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31
  • Mental Retardation, Autosomal Dominant type 31

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