PropertyValue
?:definition
  • Molecular assay reagents intended to identify mutations in the tuberous sclerosis 2 (TSC2) gene, located at chromosome 16p13.3, which is implicated as a tumor suppressor and may be involved in cell growth, arrest, and transcription mediated by steroid receptors. This inherited genetic mutation has been identified in patients with tuberous sclerosis type 2.
?:hasCUIAnnotation
?:hasGeneratedBy
?:type

Metadata

Anon_0  
expand all