Open access
Sep 2026
Clinical Application of Long‐Read Sequencing for FMR1 Gene Mutation Detection in Populations From Shandong, China
Fragile X syndrome (FXS) is a common inherited intellectual disability. In this study, long‐read sequencing was used for the FMR1 gene detection.
Yan Li, Fei Hou, Shan Shan et al.
· Molecular Genetics & Genomic... · 0 citations