Ontology highlight
ABSTRACT:
SUBMITTER: Imaizumi N
PROVIDER: S-EPMC6554220 | biostudies-literature | 2019 Aug
REPOSITORIES: biostudies-literature
Imaizumi Naoko N Takeuchi Yu Y Hirano Haruka H Torii Tomohiro T Seki Yoichi Y Morimoto Takako T Miyamoto Yuki Y Sakagami Hiroyuki H Yamauchi Junji J
Data in brief 20190524
Charcot-Marie-Tooth (CMT) diseases are genetic neuropathies in the peripheral nervous system (PNS). Type 1 CMT diseases are neuropathies in Schwann cells, PNS myelinating glial cells, whereas type 2 CMT diseases are axonal neuropathies. In addition, there are other types of categories in CMT diseases. CMT diseases are associated with approximately 100 responsible genes. Taiwanese mutation (Asn71-to-Tyr) of alanyl-tRNA synthetase (AARS) in type 2N CMT disease has been reported to have several pat ...[more]