(Q80686080)

English

An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 deletion

scientific article published on 27 July 2007

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17657515%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 deletion (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17657515%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

hereditary spastic paraplegia

1 reference

based on heuristic

inferred from title

Christian Beetz

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17657515%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

3

1 reference

Europe PubMed Central

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2 January 2020

4

1 reference

Europe PubMed Central

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2 January 2020

author name string

Anders O H Nygren

2

1 reference

Europe PubMed Central

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2 January 2020

publication date

27 July 2007

1 reference

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2 January 2020

1 reference

Europe PubMed Central

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2 January 2020

8

1 reference

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2 January 2020

4

1 reference

Europe PubMed Central

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2 January 2020

317-318

1 reference

Europe PubMed Central

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2 January 2020

https://scigraph.springernature.com/pub.10.1007/s10048-007-0099-8

0 references

Hereditary spastic paraplegia: the pace quickens

1 reference

https://pubmed.ncbi.nlm.nih.gov/17657515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17657515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development

1 reference

https://pubmed.ncbi.nlm.nih.gov/17657515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a novel SPG3A deletion in a French-Canadian family.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17657515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beginning to understand hereditary spastic paraplegia atlastin

1 reference

https://pubmed.ncbi.nlm.nih.gov/17657515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The hereditary spastic paraplegias.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17657515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

All neuropathies great and small.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17657515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

1 reference

https://pubmed.ncbi.nlm.nih.gov/17657515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-007-0099-8

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17657515%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17657515%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

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