SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (1)

Literature for OMIM 182601: SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4

Xenbase Articles:
(

Denotes literature images)

AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia., Yalcouyé A,Harmison G,Diallo S,Diallo SH,Coulibaly O,Diarra S,Ghosh S,Cissé L,Coulibaly T,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; 198:1095-953X.

AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia., Yalcouyé A,Harmison G,Diallo S,Diallo SH,Coulibaly O,Diarra S,Ghosh S,Cissé L,Coulibaly T,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; 198:1095-953X.