(Q57419078)

English

NovelSPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia

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title

NovelSPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia (English)

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main subject

hereditary spastic paraplegia

1 reference

Antonio Orlacchio

6

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Peter Henry St George-Hyslop

object named as

Peter St George-Hyslop

series ordinal

11

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Ekaterina Rogaeva

series ordinal

10

object named as

Ekaterina Rogaeva

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Toshitaka Kawarai

series ordinal

2

object named as

Toshitaka Kawarai

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Christine Sato

series ordinal

5

object named as

Christine Sato

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Shabnam Salehi-Rad

series ordinal

4

object named as

Shabnam Salehi-Rad

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Giorgio Bernardi

series ordinal

7

object named as

Giorgio Bernardi

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author name string

Satoshi Kaneko

series ordinal

1

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Edwin Yip

series ordinal

3

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Yan Liang

series ordinal

8

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Hiroshi Hasegawa

series ordinal

9

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language of work or name

English

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publication date

2006

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published in

Movement Disorders

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volume

21

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issue

9

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page(s)

1531-1533

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(Q57419078)

NovelSPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia

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