Spinocerebellar ataxia with sensory neuropathy (SCA25) (Q57970920)

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Language	Label	Description	Also known as
English	Spinocerebellar ataxia with sensory neuropathy (SCA25)	No description defined

Statements

scholarly article

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Spinocerebellar ataxia with sensory neuropathy (SCA25) (English)

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spinocerebellar ataxia

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inferred from title

Giovanni Stevanin

object named as

Giovanni Stevanin

1

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6

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Alexandra Durr

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5

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Alexis Brice

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Emmanuel Broussolle

2

object named as

Emmanuel Broussolle

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author name string

Nathalie Streichenberger

3

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Nicolas Kopp

4

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publication date

April 2005

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4

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1

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58-61

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Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity

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https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathways to motor incoordination: the inherited ataxias

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Why is SCA12 different from other SCAs?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia type 10: a disease caused by a large ATTCT repeat expansion

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of spinocerebellar ataxia type 8 (SCA8).

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features and classification of inherited ataxias.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15895562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1080/14734220510007932

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Dimensions Publication ID

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PubMed publication ID

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