Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome

Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome

Fragile X syndrome (FXS) is the leading inherited cause of intellectual disability (ID) and single gene cause of autism. Although most patients with FXS and the full mutation (FM) have complete methylation of the fragile X messenger ribonucleoprotein 1 (<i>FMR1</i>) gene, some have mosai...

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Bibliographic Details
Main Authors: YeEun Tak, Andrea Schneider, Ellery Santos, Jamie Leah Randol, Flora Tassone, Paul Hagerman, Randi J. Hagerman
Format: Article
Language:English
Published: MDPI AG 2024-03-01
Series:Genes
Subjects:
unmethylated full mutation
fragile X premutation
fragile X mosaicism
fragile X syndrome
fragile X premutation-associated conditions
Online Access:https://www.mdpi.com/2073-4425/15/3/331

Internet

https://www.mdpi.com/2073-4425/15/3/331

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