Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental Disorders
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DOI: 10.1007/s12031-020-01615-7
Abstract: TBL1XR1 is a member of the WD40 repeat-containing gene family. Mutations of TBL1XR1 have been reported in neurodevelopmental disorders (NDDs). Although the phenotypes of some patients have been described in single studies, few studies have… read more here.
Keywords: genotype phenotype; phenotype correlations; correlations tbl1xr1; tbl1xr1 neurodevelopmental ... See more keywords