(Q50349612)
English
autosomal dominant non-syndromic intellectual disability 8
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GRIN1 on chromosome 9q34.3.
- autosomal dominant mental retardation 8
- MRD8
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 8
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 8; MRD8
- Mental Retardation, Autosomal Dominant type 8
Statements
1 reference
3 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference