Mutational analysis of familial and sporadic amyotrophic lateral sclerosis withOPTNmutations in Japanese population (Q58151703)

2

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Tameko Kihira

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Sohei Yoshida

4

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Yasumasa Kokubo

5

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Shigeki Kuzuhara

6

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Hiroyuki Ishiura

7

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Masaharu Amagasa

8

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Shigeo Murayama

9

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Shoji Tsuji

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Jun Goto

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

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publication date

18 June 2012

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published in

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volume

13

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issue

6

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page(s)

562-566

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cites work

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

Mutant dynactin in motor neuron disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

?True? sporadic ALS associated with a novel SOD-1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

Mutations of optineurin in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213

Epidemiology of motor neuron disease in the Kii Peninsula of Japan, 1989–1993: Active or disappearing focus?

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/17482968.2012.684213