Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation.
Chinnery PF, Crompton DE, Birchall D, Jackson MJ, Coulthard A, Lombès A, Quinn N, Wills A, Fletcher N, Mottershead JP, Cooper P, Kellett M, Bates D, Burn J.
Chinnery PF, et al.
Brain. 2007 Jan;130(Pt 1):110-9. doi: 10.1093/brain/awl319. Epub 2006 Dec 2.
Brain. 2007.
PMID: 17142829