Complex hereditary spastic paraplegia associated with episodic visual loss caused by ACO2 variants.
Tozawa T, Nishimura A, Ueno T, Shikata A, Taura Y, Yoshida T, Nakagawa N, Wada T, Kosugi S, Uehara T, Takenouchi T, Kosaki K, Chiyonobu T.
Tozawa T, et al. Among authors: shikata a.
Hum Genome Var. 2021 Jan 26;8(1):4. doi: 10.1038/s41439-021-00136-y.
Hum Genome Var. 2021.
PMID: 33500398
Free PMC article.