SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4

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Summary

Literature (1)

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

Xenbase Articles:
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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,Lahkani SA,Donovan FX,Jacobson S,Blackstone C,Guinto CO,Landouré G,Bonifacino JS,Fischbeck KH,Grunseich C, Neurobiol Dis. May 19, 2024; :1095-953X.

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, Neurobiol Dis. May 19, 2024; :1095-953X.