(Q50349645)
English
autosomal dominant non-syndromic intellectual disability 41
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of TBL1XR1 on chromosome 3q26.32.
- autosomal dominant mental retardation 41
- MRD41
- Mental Retardation, Autosomal Dominant 41
- Mental Retardation, Autosomal Dominant type 41
Statements
1 reference
3 references
Identifiers
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1 reference
1 reference
1 reference