(Q57969491)

G. Cancel

4

0 references

Giovanni Stevanin

G. Stevanin

3

0 references

Yves Agid

18

Y. Agid

0 references

H. Ouhabi

7

H. Ouhabi

0 references

author name string

A. Benomar

1

0 references

L. Krols

2

0 references

E. LeGuern

5

0 references

G. David

6

0 references

J.-J. Martin

8

0 references

A. Dürr

9

0 references

A. Zaim

10

0 references

N. Ravisé

11

0 references

C. Busque

12

0 references

C. Penet

13

0 references

N. Van Regemorter

14

0 references

J. Weissenbach

15

0 references

M. Yahyaoui

16

0 references

T. Chkili

17

0 references

C. Van Broeckhoven

19

0 references

A. Brice

https://scigraph.springernature.com/pub.10.1038/ng0595-84

20

0 references

language of work or name

English

0 references

publication date

May 1995

0 references

published in

Nature Genetics

0 references

volume

10

0 references

issue

1

0 references

page(s)

84-88

0 references

exact match

0 references

cites work

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1 reference

A second-generation linkage map of the human genome

21 January 2018

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The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

21 January 2018

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Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I

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7 January 2021

On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family

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7 January 2021

Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy. A clinical and genetic study of eight families

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7 January 2021

Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

1 reference

7 January 2021

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

7 January 2021

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

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7 January 2021

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1 reference

7 January 2021

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

1 reference

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

7 January 2021

Avoiding recomputation in linkage analysis.

1 reference

7 January 2021

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

7 January 2021