(Q44358768)

2 December 2017

title

Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population (English)

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2 December 2017

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Nihan Erginel-Unaltuna

13

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2 December 2017

G Sevinc

5

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author name string

E Lohmann

1

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2 December 2017

B Dursun

2

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S Lesage

3

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H A Hanagasi

4

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A Honore

6

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B Bilgic

7

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H Gürvit

8

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O Dogu

9

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H Kaleagası

10

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G Babacan

11

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J Yazici

12

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A Brice

14

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M Emre

15

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publication date

10 January 2012

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European Journal of Neurology

2 December 2017

published in

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2 December 2017

volume

19

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issue

5

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2 December 2017

page(s)

769-775

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Parkinson's disease: from monogenic forms to genetic susceptibility factors

2 December 2017

cites work

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https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Mutation analysis for DJ-1 in sporadic and familial parkinsonism: screening strategy in parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

LRRK2 mutations are uncommon in Turkey.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Mutation analysis of the PINK1 gene in 391 patients with Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Prevalence and sociodemographic correlates of consanguineous marriages in Turkey

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

How much phenotypic variation can be attributed to parkin genotype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

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

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

High frequency stimulation of the subthalamic nucleus is efficacious in Parkin disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Parkin is a component of an SCF-like ubiquitin ligase complex and protects postmitotic neurons from kainate excitotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

Clinicogenetic study of mutations inLRRK2 exon 41 in Parkinson's disease patients from 18 countries

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03639.X

10.1111/J.1468-1331.2011.03639.X

21 January 2018

Identifiers

DOI

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2 December 2017

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