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

Genetic predisposition to peripheral nerve neoplasia: diagnostic criteria and pathogenesis of neurofibromatoses, Carney complex, and related syndromes

(2011) Fausto J. Rodriguez et al.   ACTA NEUROPATHOLOGICA

Molecular diagnosis and clinical onset of Charcot–Marie–Tooth disease in Japan

(2011) Akiko Abe et al.   JOURNAL OF HUMAN GENETICS

INF2Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy

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

The role of formins in human disease

(2009) Aaron D. DeWard et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

(2009) Elizabeth J Brown et al.   NATURE GENETICS

Unleashing formins to remodel the actin and microtubule cytoskeletons

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