(Q58007110)

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A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism

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A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism (English)

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parkinsonian syndrome

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Pau Pastor

2

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Eduardo Tolosa

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5

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Eduardo Tolosa

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author name string

Esteban Muñoz

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1

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Marı́a J Martı́

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3

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Rafael Oliva

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4

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language of work or name

English

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publication date

July 2000

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published in

Neuroscience Letters

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volume

289

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issue

1

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page(s)

66-68

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cites work

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

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7 January 2021

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Neuropathology of Parkinson's disease

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7 January 2021

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Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism.

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7 January 2021

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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

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7 January 2021

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Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease

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Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

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7 January 2021

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Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q.

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7 January 2021

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Familial juvenile parkinsonism: clinical and pathologic study in a family

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7 January 2021

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10.1016/S0304-3940(00)01248-9

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(Q58007110)

A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism

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