A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10) (Q24632247)

Margaret A. Pericak-Vance

inferred from title

author

10

0 references

Evan Reid

object named as

Evan Reid

1

0 references

Allison Ashley-Koch

object named as

Allison Ashley-Koch

3

0 references

Douglas A Marchuk

object named as

Douglas A Marchuk

12

1 reference

ORCID Public Data File 2021

author name string

Mark Kloos

2

0 references

Lori Hughes

4

0 references

Simon Bevan

5

0 references

Ingrid K Svenson

6

0 references

Felicia Lennon Graham

7

0 references

Perry C Gaskell

8

0 references

Andrew Dearlove

9

0 references

David C Rubinsztein

American Journal of Human Genetics

11

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language of work or name

English

0 references

publication date

November 2002

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published in

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volume

71

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issue

5

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page(s)

1189-94

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cites work

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Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

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Kinesin mutations cause motor neuron disease phenotypes by disrupting fast axonal transport in Drosophila

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https://pubmed.ncbi.nlm.nih.gov/12355402

12 December 2020

inferred from PubMed ID database lookup

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12355402

12 December 2020

inferred from PubMed ID database lookup

Hereditary spastic paraplegia: the pace quickens

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12355402

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1086/344210

1 reference

1494468

1494468

1 reference

1 reference

1 reference