Publication | Open Access

Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma

Mendelian DisorderGenetic DisorderGeneticsPathologyEarly-onset GlaucomaDegenerative DiseaseMolecular GeneticsCharcot-marie-tooth Disease AssociatedDisease Gene IdentificationNeuropathologyMedicineNew Pseudophosphatase Homologue