Gerhardt J

No ORCID on file · 1 paper in corpus
2017
Frontiers in molecular neuroscience ·doi:10.3389/fnmol.2017.00290

Fragile X syndrome (FXS), is caused by a loss-of-function mutation in the FMR1 gene located on the X-chromosome, which leads to the most common cause of inherited intellectual disability in males and the leading single-gene defect associate…