(Q57450081)

English

A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12

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title

A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12 (English)

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main subject

hereditary spastic paraplegia

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Allison E. Ashley-Koch

series ordinal

8

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Stephan Züchner

series ordinal

1

object named as

Stephan Züchner

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author name string

Melanie E. Kail

series ordinal

2

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Martha A. Nance

series ordinal

3

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Perry C. Gaskell

series ordinal

4

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Ingrid K. Svenson

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5

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Douglas A. Marchuk

series ordinal

6

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Margaret A. Pericak-Vance

series ordinal

7

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publication date

25 March 2006

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published in

Neurogenetics

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volume

7

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issue

2

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page(s)

127-129

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exact match

https://scigraph.springernature.com/pub.10.1007/s10048-006-0029-1

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cites work

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

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS10048-006-0029-1

retrieved

21 January 2018

Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16565863

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16565863

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16565863

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16565863

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S10048-006-0029-1

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PubMed ID

16565863

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(Q57450081)

A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12

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