TY  - GEN
AU  - Damián, Juan Pablo
AU  - Vázquez Alberdi, Lucia
AU  - Canclini, Lucía
AU  - Rosso, Gonzalo
AU  - Bravo, Silvia Olivera
AU  - Martínez, Mariana
AU  - Uriarte, Natalia
AU  - Ruiz, Paul
AU  - Calero, Miguel
AU  - Di Tomaso, María Vittoria
AU  - Kun, Alejandra
PY  - 2021
DO  - 10.3390/biom11040601
UR  - http://hdl.handle.net/20.500.12105/12959
AB  - Charcot-Marie-Tooth (CMT) type 1 disease is the most common human hereditary demyelinating neuropathy. Mutations in pmp22 cause about 70% of all CMT1. Trembler-J (TrJ/+) mice are an animal model of CMT1E, having the same spontaneous pmp22 mutation...
LA  - eng
PB  - Multidisciplinary Digital Publishing Institute (MDPI)
KW  - CA3 neurons
KW  - Charcot–Marie–Tooth
KW  - Trembler-J
KW  - Anxiety
KW  - Hippocampus
KW  - Peripheral-myelin-protein-22
TI  - Central Alteration in Peripheral Neuropathy of Trembler-J Mice: Hippocampal pmp22 Expression and Behavioral Profile in Anxiety Tests
TY  - research article
ER  -