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XB-PERS-4789
Publications By Salimata Diarra
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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, Lakhani SA, Donovan FX, Jacobson S, Blackstone C, Guinto CO, Landouré G, Bonifacino JS, Fischbeck KH, Grunseich C., Neurobiol Dis. August 19, 2024; 198 106537. |
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