(Q57667221)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12402269%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

title

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

1 reference

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14 December 2019

main subject

spinocerebellar ataxia

1 reference

3

1 reference

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14 December 2019

Bernard Sablonniere

12

1 reference

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14 December 2019

author name string

Isabelle Vuillaume

1

1 reference

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14 December 2019

Christian Dina

4

1 reference

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14 December 2019

Arnaud Lemainque

5

1 reference

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14 December 2019

Francis Vasseur

6

1 reference

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14 December 2019

Guy Bocquillon

7

1 reference

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14 December 2019

Patrick Devos

8

1 reference

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14 December 2019

Carole Kocinski

9

1 reference

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14 December 2019

Christiane Marzys

10

1 reference

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14 December 2019

Alain Destée

11

1 reference

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14 December 2019

David Devos

2

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14 December 2019

publication date

1 November 2002

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14 December 2019

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14 December 2019

volume

52

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14 December 2019

issue

5

1 reference

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14 December 2019

page(s)

666-670

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Recent advances in degenerative ataxias

14 December 2019

cites work

1 reference

Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Clinical features and genetic analysis of a new form of spinocerebellar ataxia

21 January 2018

1 reference

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 January 2018

1 reference

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

21 January 2018

1 reference

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?

21 January 2018

1 reference

Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Scinderin and cortical F-actin are components of the secretory machinery

21 January 2018

1 reference

Functional analyses of the transcription factor Sp4 reveal properties distinct from Sp1 and Sp3

21 January 2018

1 reference

Expression of mouse igf2 mRNA-binding protein 3 and its implications for the developing central nervous system

21 January 2018

1 reference

Autosomal dominant spinocerebellar ataxias ad infinitum?

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.10344

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12402269%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

1 reference