(Q57970906)

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A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene

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title

A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene (English)

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Isabelle Nelson

2

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Giovanni Stevanin

object named as

Giovanni Stevanin

series ordinal

6

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author name string

Michito Namekawa

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1

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Pascale Ribai

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3

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Alexandra Dürr

series ordinal

4

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Elodie Denis

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5

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Merle Ruberg

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7

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Alexis Brice

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8

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publication date

13 April 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)

131-132

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exact match

https://scigraph.springernature.com/pub.10.1007/s10048-006-0028-2

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cites work

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16612642

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16612642

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16612642

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High sensitivity mapping of methylated cytosines

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16612642

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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DOI

10.1007/S10048-006-0028-2

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PubMed publication ID

16612642

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(Q57970906)

A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene

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