ELMO2

Publications

Vargel I, et al. Hereditary intraosseous vascular malformation of the craniofacial region: an apparently novel disorder. Am J Med Genet. 2002;109(1):22-35. PMID:11932989.

Vargel I, et al. Hereditary intraosseous vascular malformation of the craniofacial region: imaging findings. Br J Radiol. 2004;77(915):197-203. PMID: 15020360.

Cetinkaya A, et al. Loss-of-function mutations in ELMO2 cause intraosseous vascular malformation by impeding RAC1 signaling. Am J Hum Genet. 2016;99(2):299-317. PMID: 27476657.

Mehawej C, et al. Homozygous mutation in ELMO2 may cause Ramon syndrome. Clin Genet. 2018;93(3):703-706. PMID: 29095483.