(Q34657227)

3 August 2017

Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families (English)

1 reference

3 August 2017

phenotypic heterogeneity

1 reference

18

0 references

Diana Zelenika

13

object named as

Diana Zelenika

1 reference

3 August 2017

Giovanni Stevanin

19

0 references

Alexandra Durr

15

object named as

Alexandra Durr

1 reference

3 August 2017

2

Naima Bouslam

1 reference

3 August 2017

16

Mohamed Yahyaoui

1 reference

3 August 2017

3

Sylvain Hanein

1 reference

3 August 2017

6

Stephan Klebe

1 reference

3 August 2017

12

Meriem Tazir

1 reference

3 August 2017

1

Nizar Elleuch

1 reference

3 August 2017

4

Alexander Lossos

1 reference

3 August 2017

5

Abdelmadjid Hamri

1 reference

3 August 2017

7

Vardiella Meiner

1 reference

3 August 2017

9

Israela Lerer

1 reference

3 August 2017

10

Djamel Grid

1 reference

3 August 2017

11

Delphine Bacq

1 reference

3 August 2017

Nezha Birouk

8

1 reference

PubMed ID

17661097

3 August 2017

Zohar Argov

14

1 reference

PubMed ID

17661097

3 August 2017

Ali Benomar

17

1 reference

3 August 2017

28 July 2007

1 reference

3 August 2017

1 reference

3 August 2017

8

1 reference

3 August 2017

4

1 reference

3 August 2017

307-315

1 reference

https://scigraph.springernature.com/pub.10.1007/s10048-007-0097-x

3 August 2017

0 references

cites work

Familial Spastic Paraplegia with Amyotrophy, Oligophrenia, and Central Retinal Degeneration

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-007-0097-X

SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-007-0097-X

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.

21 January 2018

1 reference

12 December 2020

Classification of the hereditary ataxias and paraplegias

1 reference

12 December 2020

Allegro, a new computer program for multipoint linkage analysis

1 reference

12 December 2020

Advances in the hereditary spastic paraplegias

1 reference

12 December 2020

Faster sequential genetic linkage computations

1 reference

12 December 2020

Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.

1 reference

12 December 2020

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

12 December 2020

Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia

1 reference

12 December 2020

Hereditary spastic paraplegia

1 reference

12 December 2020

Two families with autosomal recessive spastic paraplegia, pigmented maculopathy, and dementia

1 reference

12 December 2020

10.1007/S10048-007-0097-X

Identifiers

DOI

1 reference

3 August 2017

1 reference

PubMed ID

17661097