SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

(2010) H. Skre   CLINICAL GENETICS

Congenital Hypomyelinating Neuropathy with Lethal Conduction Failure in Mice Carrying the Egr2 I268N Mutation

(2009) R. H. Baloh et al.   JOURNAL OF NEUROSCIENCE

The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy

(2009) Henry Houlden et al.   NEUROMUSCULAR DISORDERS

Rab and Arl GTPase Family Members Cooperate in the Localization of the Golgin GCC185

(2008) Alondra Schweizer Burguete et al.   CELL

Molecular mechanisms of inherited demyelinating neuropathies

(2008) Steven S. Scherer et al.   GLIA

Glial and neuronal isoforms of Neurofascin have distinct roles in the assembly of nodes of Ranvier in the central nervous system

(2008) Barbara Zonta et al.   JOURNAL OF CELL BIOLOGY

Efficient termination of vacuolar Rab GTPase signaling requires coordinated action by a GAP and a protein kinase

(2008) Christopher L. Brett et al.   JOURNAL OF CELL BIOLOGY

Distinct endocytic recycling of myelin proteins promotes oligodendroglial membrane remodeling

(2008) C. Winterstein et al.   JOURNAL OF CELL SCIENCE

Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster

(2008) Isabelle Gosselin et al.   NEUROMUSCULAR DISORDERS