FAM66B
Contents
Annotation
Name
FAM66B
Alias
FAM66E
Disease
Disease: hereditary haemorrhagic telangiectasia (PMID:24603890)
Dysfunction type: expression
Description: Top 42 long non-coding RNAs (q<0.001) differentially expressed in HHT telangiectasia.
Function
Function Mechanism: NA (PMID:24603890)
Biological Process: pathogenic process
Description: therapy target
