(Q57419055)

6

object named as

E. Rogaeva

0 references

Toshitaka Kawarai

2

object named as

T. Kawarai

0 references

author name string

M. Matsui

1

0 references

Y. Hase

3

0 references

H. Tomimoto

4

0 references

K. Iseki

5

0 references

G. Bernardi

8

0 references

P. St. George-Hyslop

9

0 references

R. Takahashi

10

0 references

M. Matsui

PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier

11

0 references

publication date

22 March 2007

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published in

Journal of Neurology

0 references

volume

254

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issue

7

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page(s)

972-974

0 references

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00415-006-0446-Y

Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia

21 January 2018

1 reference

12 December 2020

The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathy.

1 reference

12 December 2020

Clinical and genetic study of a large Italian family linked to SPG12 locus

1 reference

12 December 2020

Cellular Localization, Oligomerization, and Membrane Association of the Hereditary Spastic Paraplegia 3A (SPG3A) Protein Atlastin

1 reference

12 December 2020

Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

1 reference

12 December 2020

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

1 reference

12 December 2020

Hereditary spastic paraplegia: clinical genetic study of 15 families

1 reference

12 December 2020

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

1 reference

12 December 2020