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Autor:
Vinita G. Chittoor, Lee Sooyeon, Sunitha Rangaraju, Jessica R. Nicks, Jordan T. Schmidt, Irina Madorsky, Diana C. Narvaez, Lucia Notterpek
Publikováno v:
ASN Neuro, Vol 5 (2013)
Charcot–Marie–Tooth disease type 1A (CMT1A) is a hereditary demyelinating neuropathy linked with duplication of the peripheral myelin protein 22 ( PMP22 ) gene. Transgenic C22 mice, a model of CMT1A, display many features of the human disease, in
Externí odkaz:
https://doaj.org/article/48ad42821b82448abca2e113d6cd0950