AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Diarra S, Ghosh S, Cissé L, Coulibaly T, Yalcouyé A, Harmison G, Diallo S, Diallo SH, Coulibaly O, Schindler A, Cissé CAK, Maiga AB, Bamba S, Samassekou O, Khokha MK, Mis EK, Lahkani SA, Donovan FX, Jacobson S, Blackstone C, Guinto CO, Landouré G, Bonifacino JS, Fischbeck KH, Grunseich C.
Diarra S, et al. Among authors: coulibaly o.
Neurobiol Dis. 2024 May 19:106537. doi: 10.1016/j.nbd.2024.106537. Online ahead of print.
Neurobiol Dis. 2024.
PMID: 38772452