https://medlineplus.gov/genetics/condition/mn1-c-terminal-truncation-syndrome/
MN1 C-terminal truncation syndrome: MedlinePlus Genetics
MN1 C-terminal truncation (MCTT) syndrome is a condition characterized by intellectual disability, developmental delay, distinctive facial features, and brain...
mn1cterminalsyndromemedlineplus
https://medlineplus.gov/genetics/gene/mn1/
MN1 gene: MedlinePlus Genetics
The MN1 gene provides instructions for making a protein whose function is unclear. Learn about this gene and related health conditions.
mn1 genemedlineplusgenetics
https://www.ncbi.nlm.nih.gov/books/NBK560443/
MN1 C-Terminal Truncation Syndrome - GeneReviews® - NCBI Bookshelf
Individuals with MN1 C-terminal truncation (MCTT) syndrome have mild-to-moderate intellectual disability, severe expressive language delay, dysmorphic facial...
ncbi bookshelfmn1terminaltruncationsyndrome