Novel myelin protein zero mutation (Arg36Trp) in a patient with acute onset painful neuropathy

Shy, 2005, Hereditary motor and sensory neuropathies related to MPZ (P0) mutations, 1681 Szabo, 2005, Marked phenotypic variation in a family with a new myelin protein zero mutation, Neuromuscul Disord, 15, 760, 10.1016/j.nmd.2005.07.006 Shapiro, 1996, Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin, Neuron, 17, 435, 10.1016/S0896-6273(00)80176-2 Dyck, 1981, Intensive evaluation of referred unclassified neuropathies yields improved diagnosis, Ann Neurol, 10, 222, 10.1002/ana.410100304 De Jonghe, 1999, The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-tooth phenotype, Brain, 122, 281, 10.1093/brain/122.2.281 Shy, 2004, Phenotypic clustering in MPZ mutations, Brain, 127, 371, 10.1093/brain/awh048 Donaghy, 2000, Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation, J Neurol Neurosurg Psych, 69, 799, 10.1136/jnnp.69.6.799 Watanabe, 2002, Corticosteroid-responsive asymmetric neuropathy with a myelin protein zero gene mutation, Neurology, 59, 767, 10.1212/WNL.59.5.767 Shy, 1997, Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP), J Neuropathol Exp Neurol, 56, 811, 10.1097/00005072-199756070-00008 Schmid, 2000, Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance, J Neurosci, 20, 729, 10.1523/JNEUROSCI.20-02-00729.2000