(Q46742950)

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19 January 2020

title

FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion (English)

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19 January 2020

1

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19 January 2020

Hitoshi Warita

3

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19 January 2020

Tetsuya Akiyama

7

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19 January 2020

author name string

Masashi Aoki

2

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19 January 2020

Masaaki Kato

4

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19 January 2020

Hideki Mizuno

5

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19 January 2020

Naoko Shimakura

6

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19 January 2020

Hirokazu Furuya

8

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19 January 2020

Toshihiro Hokonohara

9

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19 January 2020

Akiko Iwaki

10

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19 January 2020

Shinji Togashi

11

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19 January 2020

Hidehiko Konno

12

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19 January 2020

Yasuto Itoyama

13

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19 January 2020

publication date

12 March 2010

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Journal of Human Genetics

19 January 2020

published in

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19 January 2020

volume

55

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19 January 2020

issue

4

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19 January 2020

page(s)

252-254

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https://scigraph.springernature.com/pub.10.1038/jhg.2010.16

19 January 2020

exact match

0 references

cites work

Molecular biology of amyotrophic lateral sclerosis: insights from genetics

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

Another gene for ALS: mutations in sporadic cases and the rare variant hypothesis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

Mutations in FUS cause FALS and SALS in French and French Canadian populations

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

Mutations of FUS gene in sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

Induced ncRNAs allosterically modify RNA-binding proteins in cis to inhibit transcription

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

FUS pathology in basophilic inclusion body disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

A new subtype of frontotemporal lobar degeneration with FUS pathology

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

Rethinking ALS: the FUS about TDP-43.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.16

7 January 2021

Identifiers

DOI

10.1038/JHG.2010.16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20224596%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference