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Publications by Alexandra Dürr

SCA15 Due to Large ITPR1 Deletions in a Cohort of 333 White Families With Dominant Ataxia

Archives of Neurology

English

A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-Q34

American Journal of Human Genetics

English

Origin of the Mutations in the Parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, Whereas Point Mutations May Result From Founder Effects

American Journal of Human Genetics

English

Hereditary Spastic Paraplegia SPG13 Is Associated With a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60

American Journal of Human Genetics

English

Juvenile-Onset Parkinsonism as a Result of the First Mutation in the Adenosine Triphosphate Orientation Domain of PINK1

Archives of Neurology

English

Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia

Archives of Neurology

English

Les Tests Présymptomatiques en Neurogénétique

Medecine/Sciences

Molecular Biology

English