A novelINF2mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis

(2013) Kentaro Toyota et al.   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

Clinical implications of genetic advances in Charcot–Marie–Tooth disease

(2013) Alexander M. Rossor et al.   Nature Reviews Neurology

De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy

(2013) I. Mademan et al.   NEUROLOGY

Novel INF2 mutation p. L77P in a family with glomerulopathy and Charcot-Marie-Tooth neuropathy

(2012) Patricia Q. Rodriguez et al.   PEDIATRIC NEPHROLOGY

INF2Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy

(2011) Olivia Boyer et al.   NEW ENGLAND JOURNAL OF MEDICINE

Focal Segmental Glomerulosclerosis

(2011) Vivette D. D'Agati et al.   NEW ENGLAND JOURNAL OF MEDICINE

Unleashing formins to remodel the actin and microtubule cytoskeletons

(2009) Melissa A. Chesarone et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY