https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2023.1141488/full
Frontiers | Case Report: A novel heterozygous nonsense mutation in KRIT1 cause hereditary cerebral...
Cerebral cavernous malformation (CCM) is a vascular malformation of the central nervous system and mainly characterized by enlarged capillary cavities withou...
https://pubchem.ncbi.nlm.nih.gov/gene/Krit1/rat
Krit1 (Norway rat) | Gene Target - PubChem
Gene target information for Krit1 - KRIT1, ankyrin repeat containing (Norway rat). Find diseases associated with this biological target and compounds tested...
norway ratgenetargetpubchem