Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype.
Bayrakli F, Guclu B, Yakicier C, Balaban H, Kartal U, Erguner B, Sagiroglu MS, Yuksel S, Ozturk AR, Kazanci B, Ozum U, Kars HZ.
Bayrakli F, et al. Among authors: kars hz.
BMC Genet. 2013 Sep 28;14:95. doi: 10.1186/1471-2156-14-95.
BMC Genet. 2013.
PMID: 24073994
Free PMC article.