(Q37298549)

19 August 2017

Comprehensive phenotype of the p.Arg420his allelic form of spinocerebellar ataxia type 13. (English)

1 reference

19 August 2017

spinocerebellar ataxia

1 reference

1 reference

S H Subramony

1

1 reference

19 August 2017

Joel Advincula

2

1 reference

19 August 2017

Susan Perlman

3

1 reference

19 August 2017

Raymond L Rosales

4

1 reference

19 August 2017

Lillian V Lee

5

1 reference

19 August 2017

Tetsuo Ashizawa

6

1 reference

19 August 2017

Michael F Waters

7

1 reference

19 August 2017

1 December 2013

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19 August 2017

1 reference

19 August 2017

12

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19 August 2017

6

1 reference

19 August 2017

932-936

1 reference

Creative Commons Attribution 2.0 Generic

19 August 2017

start time

3 August 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1007/s12311-013-0507-6

0 references

cites work

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

Overview of autosomal dominant ataxias

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

Update on degenerative ataxias

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

Scale for the assessment and rating of ataxia: development of a new clinical scale

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

Mesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13).

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

Oculomotor and visual axis systems sparing in spinocerebellar ataxia type 13(R420H).

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

Measuring Friedreich ataxia: Interrater reliability of a neurologic rating scale.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3824261

10.1007/S12311-013-0507-6

2 September 2018

Identifiers

DOI

1 reference

19 August 2017

1 reference

19 August 2017

1 reference