We describe a Japanese family in which inheritance of a novel mutation p.A100T in SPG6 resulted in an autosomal dominant form of hereditary spastic paraplegia (ADHSP). Clinical investigation showed a pure form of HSP. Our study demonstrates further allelic heterogeneity of SPG6.

Kaneko, S., Kawarai, T., Yip, E., Salehi Rad, S., Sato, C., Orlacchio, A., et al. (2006). Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia. MOVEMENT DISORDERS, 21(9), 1531-1533 [10.1002/mds.21005].

Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia

ORLACCHIO, ANTONIO;BERNARDI, GIORGIO;
2006-09-01

Abstract

We describe a Japanese family in which inheritance of a novel mutation p.A100T in SPG6 resulted in an autosomal dominant form of hereditary spastic paraplegia (ADHSP). Clinical investigation showed a pure form of HSP. Our study demonstrates further allelic heterogeneity of SPG6.
set-2006
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/26 - NEUROLOGIA
English
Con Impact Factor ISI
Protein Structure, Secondary; DNA Mutational Analysis; Humans; Neurologic Examination; Membrane Proteins; Polymerase Chain Reaction; Alleles; Heterozygote Detection; Polymorphism, Restriction Fragment Length; Spastic Paraplegia, Hereditary; Adult; Protein Structure, Tertiary; Amino Acid Substitution; Male
Kaneko, S., Kawarai, T., Yip, E., Salehi Rad, S., Sato, C., Orlacchio, A., et al. (2006). Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia. MOVEMENT DISORDERS, 21(9), 1531-1533 [10.1002/mds.21005].
Kaneko, S; Kawarai, T; Yip, E; Salehi Rad, S; Sato, C; Orlacchio, A; Bernardi, G; Liang, Y; Hasegawa, H; Rogaeva, E; St George Hyslop, P
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/28308
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