Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia (Q34496114)

2 August 2017

title

Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia (English)

1 reference

2 August 2017

Marcia A Blair

1

1 reference

2 August 2017

Shaochun Ma

series ordinal

2

1 reference

2 August 2017

Peter Hedera

series ordinal

3

1 reference

2 August 2017

publication date

18 February 2006

1 reference

2 August 2017

1 reference

2 August 2017

volume

7

1 reference

2 August 2017

issue

1

1 reference

2 August 2017

page(s)

47-50

1 reference

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group

2 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-005-0027-8

SPG3A: An additional family carrying a new atlastin mutation

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-005-0027-8

Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-005-0027-8

Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia

21 January 2018

1 reference

12 December 2020

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

1 reference

12 December 2020

The hereditary spastic paraplegias: nine genes and counting

1 reference

12 December 2020

Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A.

1 reference

12 December 2020

Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia

1 reference

12 December 2020

Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia. A clinical and molecular genetic study of 28 United Kingdom families

1 reference

12 December 2020

Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus

1 reference

12 December 2020

Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class.

1 reference

12 December 2020

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

1 reference

12 December 2020

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

1 reference

12 December 2020

Prediction of deleterious human alleles

1 reference

12 December 2020

Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q.

1 reference

12 December 2020

Kinesin molecular motors: transport pathways, receptors, and human disease

1 reference

12 December 2020

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

1 reference

12 December 2020

Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation

1 reference

12 December 2020

Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia

1 reference

12 December 2020

10.1007/S10048-005-0027-8

Identifiers

DOI

1 reference

2 August 2017

1 reference