(Q47882965)

6 February 2018

title

Cloning and distribution of the rat parkin mRNA. (English)

1 reference

6 February 2018

author

Sebastiano Cavallaro

series ordinal

3

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6 February 2018

author name string

V D'Agata

series ordinal

1

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6 February 2018

W Zhao

series ordinal

2

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6 February 2018

publication date

1 February 2000

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6 February 2018

published in

Molecular Brain Research

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6 February 2018

volume

75

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6 February 2018

issue

2

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6 February 2018

page(s)

345-349

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6 February 2018

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

The primary structure of rat ribosomal protein S18.

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https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

7 January 2021

Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

7 January 2021

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene

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https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

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https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

7 January 2021

Familial juvenile parkinsonism: clinical and pathologic study in a family

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

7 January 2021

https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

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7 January 2021

Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

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https://api.crossref.org/works/10.1016%2FS0169-328X%2899%2900286-7

7 January 2021

10.1016/S0169-328X(99)00286-7

Identifiers

DOI

1 reference

6 February 2018

1 reference

6 February 2018