(Q34386808)

1 August 2017

title

Genetics of Parkinson's disease: the yield (English)

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1 August 2017

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Marianna Spatola

1

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1 August 2017

Christian Wider

series ordinal

2

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1 August 2017

publication date

1 January 2014

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Parkinsonism and Related Disorders

1 August 2017

published in

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1 August 2017

volume

20 Suppl 1

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1 August 2017

page(s)

S35-8

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The role of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Olfactory dysfunction in LRRK2 G2019S mutation carriers

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Gait alterations in healthy carriers of the LRRK2 G2019S mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

VPS35 mutations in Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Frequency of the D620N mutation in VPS35 in Parkinson disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Translation initiator EIF4G1 mutations in familial Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Study of the genetic variability in a Parkinson's Disease gene: EIF4G1

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

How much phenotypic variation can be attributed to parkin genotype?

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

PLA2G6 mutation underlies infantile neuroaxonal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Characterization of PLA2G6 as a locus for dystonia-parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicity

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

The utility F-box for protein destruction

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Cellular regulation and proposed biological functions of group VIA calcium-independent phospholipase A2 in activated cells

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

LRRK2 low-penetrance mutations (Gly2019Ser) and risk alleles (Gly2385Arg)-linking familial and sporadic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Association of the MAPT locus with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

Evidence for more than one Parkinson's disease-associated variant within the HLA region

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970011-7

7 January 2021

10.1016/S1353-8020(13)70011-7

Identifiers

DOI

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1 August 2017

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