HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

human GLI3 protein

defects in GLI3 are a cause of: PALLISTER-HALL SYNDROME, type a1/b postaxial polydactyly (PAPA1/PAPB), and type IV preaxial polydactyly; RefSeq NM_000168
Also Known As:
GLI3 protein, human; GLI-Kruppel family member GLI3 (Greig cephalopolysyndactyly syndrome) protein, human
Networked: 0 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results