(Q28216308)

13

object named as

J Hardy

0 references

Sarah Lincoln

5

object named as

S Lincoln

0 references

Matthew J. Farrer

1

object named as

M Farrer

0 references

author name string

P Chan

2

0 references

R Chen

3

0 references

L Tan

4

0 references

L Forno

7

0 references

L Petrucelli

9

0 references

J Hussey

10

0 references

A Singleton

11

0 references

C Tanner

12

0 references

J W Langston

14

0 references

D Hernandez

Clinical and neuropathological aspects of autosomal recessive juvenile parkinsonism.

6

0 references

language of work or name

English

0 references

publication date

September 2001

0 references

published in

Annals of Neurology

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volume

50

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page(s)

293-300

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issue

3

0 references

cites work

1 reference

Diagnostic criteria for Parkinson disease

21 January 2018

1 reference

Familial juvenile parkinsonism: clinical and pathologic study in a family.

21 January 2018

1 reference

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

21 January 2018

1 reference

Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients

21 January 2018

1 reference

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

21 January 2018

1 reference

21 January 2018

RING for destruction?

1 reference

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

21 January 2018

1 reference

Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene

21 January 2018

1 reference

Association between early-onset Parkinson's disease and mutations in the parkin gene

21 January 2018

1 reference

Core assessment program for intracerebral transplantations (CAPIT)

21 January 2018

1 reference

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

21 January 2018

1 reference

Widespread alterations of alpha-synuclein in multiple system atrophy

21 January 2018

1 reference

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

21 January 2018

1 reference

Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects

21 January 2018

1 reference

Differential expression of the parkin gene in the human brain and peripheral leukocytes

21 January 2018

1 reference

Molecular cloning, gene expression, and identification of a splicing variant of the mouse parkin gene

21 January 2018

1 reference

Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.1132

1 reference

Consolidated OpenCitations Corpus – April 2017

2252790

2252790

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference