1 Die subzelluläre Lokalisation und Wirkung auf a-Tubulin von ...

Hughes C.A., Byrne P.C., Webb S., McMonagle P., Patterson V., Hutchinson M., Parfrey
N.A., SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q.
Neurology 2001, 56, 1230–3
Jouet M, Rosenthal A, Armstrong G et al.: X-Iinked spastic paraplegia (SPG1), MASA
syndrome and X-linked hydrocephalus result from mutations in the L1 gene. Nature
Genet 1994; 7: 402-407.
Kammermeier L., Spring J., Stierwald M., Burgunder J.M., Reichert H., Identification of the
Drosophila melanogaster homolog of the human spastin gene., Dev Genes Evol. Aug 2003,
213(8), 412-5
Mannan A.U., Boehm j., Sauter S.M., Rauber A., Byrne P.C., Neesen J., Engel W., Spastin,
The most commonly mutated protein in hereditary spastic paraplegia interacts with
Reticulon1 an endoplasmatic reticulum protein. Neurogenetics 2006 May, 7 (2), 93-103
Mc Dermott C. J., Grierson a. J., et al, Hereditary Spastic Paraparesis: Disrupted Intracellular
Transport Associated with Spastin Mutation, Ann Neurol 2003; 54; 748-759
Meijer IA, Cossette P, Roussel J, Benard M, Toupin S, Rouleau GA, A novel locus for pure
recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1. Ann Neurol. 2004 Oct,
56(4), 579-82
Orlacchio A, Kawarai T, Gaudiello F, St George-Hyslop PH, Floris R, Bernardi G, New locus
for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1. Ann Neurol. 2005 Sep,
58(3), 423-9
Patel S., Latterich M. The AAA team: related ATPases with diverse functions. Cell Biol
1998, 8, 65-71.
Patel H., Hart P.E., Warner T.T., Houlston R.S., Patton M.A., Jeffery S., Crosby A.H., The
Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14,
with evidence for genetic heterogeneity within this subtype. Am J Hum Genet 2001, 69, 209–
15
55