Hereditary spastic paraplegia: the pace quickens (Q74448167)

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10 November 2019

editorial

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title

Hereditary spastic paraplegia: the pace quickens (English)

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hereditary spastic paraplegia

10 November 2019

main subject

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John K Fink

1

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10 November 2019

publication date

1 June 2002

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10 November 2019

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10 November 2019

volume

51

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issue

6

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10 November 2019

page(s)

669-672

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Classification of the hereditary ataxias and paraplegias

10 November 2019

cites work

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Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34

21 January 2018

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Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation

21 January 2018

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

21 January 2018

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

21 January 2018

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Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome

21 January 2018

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

21 January 2018

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Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia

21 January 2018

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Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

21 January 2018

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A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3

21 January 2018

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Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

21 January 2018

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Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/ANA.10258

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10 November 2019

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