MEOX1

Publications

Mohamed JY et al. Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly. Am J Hum Genet. 2013;92(1):157-61.  PMID: 23290072.

Bayrakli F et al. Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype. BMC Genet. 2013;14(1):95.  PMID: 24073994.