ADGRG6

Publications

Bayram et al. Molecular etiology of arthrogryposis families of mostly Turkish origin. J Clin Invest. 2016;126(2):762-78.  PMID: 26752647.

Hosseini M et al. GPR126: A novel candidate gene implicated in autosomal recessive intellectual disability. Am J Med Genet A. 2019;179(1):13-19.  PMID: PMID: 30549416.

Ravenscroft G et al. Mutations in GPR126 cause severe arthrogryposis multiplex congenita. Am J Hum Genet. 2015;96(6):955-61.  PMID: 26004201.