Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Tarpey, P., Thomas, S., Sarvananthan, N., Mallya, U., Lisgo, S., Talbot, C.J., Roberts, E.O., Awan, M., Surendran, M., McLean, R.J., Reinecke, R.D., Langmann, A., et al.: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.  Nature Genet. 38: 1242-1244, 2006.