BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes

Khani, M; Shamshiri, H; Taheri, H; Hardy, J; Bras, JT; Carmona, S; Moazzeni, H; Alavi, A; Heshmati, A; Taghizadeh, P; Nilipour, Y; Ghazanfari, T; Shahabi, M; Okhovat, AA; Rohani, M; Valle, G; Boostani, R; Abdi, S; Eshghi, S; Nafissi, S; Elahi, E

Elahi, E (corresponding author), Univ Tehran, Coll Sci, Sch Biol, Enghelab Ave, Tehran 1417614411, Iran.; Nafissi, S (corresponding author), Univ Tehran Med Sci, Iranian Ctr Neurol Res, Neurosci Inst, Tehran, Iran.; Nafissi, S (corresponding author), Univ Tehran Med Sci, Dept Neurol, Tehran, Iran.

NEUROBIOLOGY OF AGING, 2021; 99 ():

Abstract

Brown-Vialetto-Van Laere (BVVL) and Fazio-Londe are disorders with amyotrophic lateral sclerosis-like features, usually with recessive inheritance. We......

Full Text Link


Links

期刊讨论 | 中国SCI论文 | 期刊主页 | 投稿经验 | 杂志官网 | 投稿链接 | 作者需知 | PMC链接 | Pubmed全文检索