(Q34354126)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15455264%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

title

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families (English)

1 reference

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autosomal dominant cerebellar ataxia type III

3 January 2020

main subject

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author

Kazuhito Tsuruta

7

1 reference

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3 January 2020

author name string

Ryuki Hirano

1

1 reference

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3 January 2020

Hiroshi Takashima

2

1 reference

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3 January 2020

Ryuichi Okubo

3

1 reference

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3 January 2020

Keiko Tajima

4

1 reference

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3 January 2020

Yuji Okamoto

5

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3 January 2020

Shimon Ishida

6

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3 January 2020

Takayo Arisato

8

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3 January 2020

Hitoshi Arata

9

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3 January 2020

Masanori Nakagawa

10

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3 January 2020

Mitsuhiro Osame

11

1 reference

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3 January 2020

Kimiyoshi Arimura

12

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3 January 2020

publication date

29 September 2004

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3 January 2020

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3 January 2020

volume

5

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3 January 2020

issue

4

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3 January 2020

page(s)

215-221

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https://scigraph.springernature.com/pub.10.1007/s10048-004-0194-z

3 January 2020

exact match

0 references

cites work

A new autosomal dominant pure cerebellar ataxia.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-004-0194-Z

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.

21 January 2018

1 reference

12 December 2020

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.

1 reference

12 December 2020

A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1

1 reference

12 December 2020

Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.

1 reference

12 December 2020

Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region

1 reference

12 December 2020

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

1 reference

12 December 2020

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

12 December 2020

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

1 reference

12 December 2020

Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia

1 reference

12 December 2020

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

1 reference

12 December 2020

Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1

1 reference

12 December 2020

Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)

1 reference

12 December 2020

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

1 reference

12 December 2020

A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1.

1 reference

12 December 2020

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

1 reference

12 December 2020

Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation

1 reference

12 December 2020

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

12 December 2020

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan

1 reference

12 December 2020

Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant

1 reference

12 December 2020

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

1 reference

12 December 2020

Easy calculations of lod scores and genetic risks on small computers

1 reference

12 December 2020

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

1 reference

12 December 2020

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

1 reference

12 December 2020

Clinical features and classification of inherited ataxias.

1 reference

12 December 2020

Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.

1 reference

12 December 2020

A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia

1 reference

12 December 2020

Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20.

1 reference

12 December 2020

A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]

1 reference

12 December 2020

A form of inherited cerebellar ataxia with saccadic intrusions, increased saccadic speed, sensory neuropathy, and myoclonus.

1 reference

12 December 2020

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

1 reference

12 December 2020

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

12 December 2020

Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.

1 reference

12 December 2020

10.1007/S10048-004-0194-Z

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15455264%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference