G. David

发表

The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.

J. Weissenbach, Y. Agid, A. Brice, 1996, American journal of human genetics.

An expanded CAG repeat sequence in spinocerebellar ataxia type 7.

H. Ehrsson, K. Lindblad, A. Brice, 1996, Genome research.

Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G3145TG/A3145TG)

Y. Agid, A. Durr, A. Dürr, 1999, European Journal of Human Genetics.

Clinical and molecular features of spinocerebellar ataxia type 6

Y. Agid, S. Rivaud, A. Dürr, 1997, Neurology.

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

Y. Agid, M. Ruberg, G. Yvert, 1997, Nature Genetics.

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

Y. Agid, A. Brice, G. Stevanin, 1995, Nature.

Spinocerebellar ataxia type 7 (SCA7)

M. Ruberg, C. Duyckaerts, A. Durr, 2020, Analysis of Triplet Repeat Disorders.

Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).

Y. Agid, A. Dürr, A. Brice, 1998, Human molecular genetics.

Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1–14.1

C. Broeckhoven, A. Dürr, A. Brice, 1997, Human Genetics.

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

J. Weissenbach, Y. Agid, C. Broeckhoven, 1995, Nature Genetics.

Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutation.

A. Brice, G. Stevanin, N. Wood, 1999, American journal of human genetics.

Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.

Y. Agid, A. Durr, T. Klockgether, 1996, Human molecular genetics.

De novo expansion of intermediate alleles in spinocerebellar ataxia 7.

M. Ruberg, A. Durr, A. Dürr, 1998, Human molecular genetics.