Dominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathology

Charcot-Marie-Tooth (CMT) neuropathies are collectively the most common hereditary neurological condition and a major health burden for society. Dominant mutations in the gene GARS, encoding the ubiquitous enzyme, glycyl-tRNA synthetase (GlyRS), cause peripheral nerve degeneration and lead to CMT di...

詳細記述

書誌詳細
主要な著者: Grice, S, Sleigh, J, Motley, W, Liu, J, Burgess, R, Talbot, K, Cader, M
フォーマット: Journal article
言語:English
出版事項: Oxford University Press 2015