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

Autor: Tarpey, Patrick, Thomas, Shery, Sarvananthan, Nagini, Mallya, Uma, Lisgo, Steven, Talbot, Chris J, Roberts, Eryl O, Awan, Musarat, Surendran, Mylvaganam, McLean, Rebecca J, Reinecke, Robert D, Langmann, Andrea, Lindner, Susanne, Koch, Martina, Jain, Sunila, Woodruff, Geoffrey, Gale, Richard P, Degg, Chris, Droutsas, Konstantinos, Asproudis, Ioannis
Předmět:
Zdroj: Nature Genetics; Jul2011, Vol. 43 Issue 7, p720-720, 1p
Abstrakt: A correction to the article "Mutations in FRMD7, a Newly Identified Member of the FERM Family, Cause X-Linked Idiopathic Congenital Nystagmus," that was published online October 1, 2006 issue and appeared in the November 2006 printed edition is presented.
Databáze: Complementary Index