(Q46551452)

23 December 2017

title

LRRK2: bridging the gap between sporadic and hereditary Parkinson's disease (English)

1 reference

23 December 2017

1

Elbaz A

1 reference

23 December 2017

language of work or name

English

0 references

publication date

6 June 2008

1 reference

23 December 2017

published in

Lancet Neurology

1 reference

23 December 2017

volume

7

1 reference

23 December 2017

issue

7

1 reference

23 December 2017

page(s)

562-564

1 reference

23 December 2017

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970118-2

7 January 2021

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970118-2

7 January 2021

Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson's disease cohort.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970118-2

7 January 2021

Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970118-2

7 January 2021

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970118-2

7 January 2021

Evaluation of LRRK2 G2019S penetrance: Relevance for genetic counseling in Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970118-2

7 January 2021

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970118-2

7 January 2021

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970118-2

7 January 2021

10.1016/S1474-4422(08)70118-2

Identifiers

DOI

1 reference

23 December 2017

PubMed ID

18539536

1 reference

23 December 2017