AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia

Autor: Diarra, Salimata, Ghosh, Saikat, Cissé, Lassana, Coulibaly, Thomas, Yalcouyé, Abdoulaye, Harmison, George, Diallo, Salimata, Diallo, Seybou H., Coulibaly, Oumar, Schindler, Alice, Cissé, Cheick A.K., Maiga, Alassane B., Bamba, Salia, Samassekou, Oumar, Khokha, Mustafa K., Mis, Emily K., Lakhani, Saquib A., Donovan, Frank X., Jacobson, Steve, Blackstone, Craig, Guinto, Cheick O., Landouré, Guida, Bonifacino, Juan S., Fischbeck, Kenneth H., Grunseich, Christopher
Zdroj: In Neurobiology of Disease August 2024 198
Databáze: ScienceDirect
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