(Q51029887)

27 March 2018

title

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families. (English)

1 reference

27 March 2018

autosomal dominant cerebellar ataxia type I

main subject

0 references

author

Giovanni Stevanin

3

1 reference

27 March 2018

Hervé Chneiweiss

10

1 reference

27 March 2018

Geraldine Cancel-Tassin

object named as

G Cancel

2

0 references

Yves Agid

11

object named as

Y Agid

1 reference

27 March 2018

A Lezin

1

1 reference

27 March 2018

D Smadja

4

1 reference

27 March 2018

J C Vernant

5

1 reference

27 March 2018

A Dürr

6

1 reference

27 March 2018

J Martial

7

1 reference

27 March 2018

G G Buisson

8

1 reference

27 March 2018

R Bellance

9

1 reference

27 March 2018

A Brice

12

1 reference

27 March 2018

publication date

1 May 1996

1 reference

27 March 2018

published in

Human Genetics

1 reference

27 March 2018

volume

97

1 reference

27 March 2018

issue

5

1 reference

27 March 2018

page(s)

671-676

1 reference

27 March 2018

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)

cites work

1 reference

12 December 2020

Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23–q24.1

1 reference

12 December 2020

Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity

1 reference

12 December 2020

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region

1 reference

12 December 2020

The gene for Machado-Joseph disease maps to human chromosome 14q

1 reference

12 December 2020

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers

1 reference

12 December 2020

Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba

1 reference

12 December 2020

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

1 reference

12 December 2020

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

12 December 2020

Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus

1 reference

12 December 2020

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus

1 reference

12 December 2020

Letter: Hereditary ataxia and HL-A genotypes

1 reference

12 December 2020

The 1993-94 Généthon human genetic linkage map

1 reference

12 December 2020

Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2).

1 reference

12 December 2020

Anticipation in spinocerebellar ataxia type 2

1 reference

12 December 2020

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

1 reference

12 December 2020

SCA2 is not a major locus for ADCA type I in French families

1 reference

12 December 2020

Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French families.

1 reference

12 December 2020

A routine method for the establishment of permanent growing lymphoblastoid cell lines

1 reference

12 December 2020

Clinical features and classification of inherited ataxias.

1 reference

12 December 2020

A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus

1 reference

12 December 2020

Analysis of the SCAI CAG repeat in a large number of families with dominant ataxia: Clinical and molecular correlations

1 reference

12 December 2020

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

12 December 2020

Identifiers

DOI

10.1007/S004390050114

1 reference

27 March 2018

1 reference

27 March 2018