About: LRRK2 and Parkinson?s disease in Norway

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scientific article published on 01 January 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique (publié 2007) (fr) наукова стаття, опублікована в травні 2007 (uk) im Jahr 2007 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 2007 (ast) artikull shkencor i botuar më 01 janar 2007 (sq) scientific article published on 01 January 2007 (en)
publication date	wds:Q57983263-13D1D3CF-CB08-48CA-81A7-46700B60A78F
publication date	2007-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57983263-B3B4EA27-2219-4E90-8820-6A4E2E2716FB
language of work or name	English
cites work	wds:Q57983263-0E74F1E3-F693-43D2-AA81-D98C934AEF78 wds:Q57983263-11040D42-00A2-451A-B775-07081FB1D192 wds:Q57983263-170B676B-AEA1-4D19-A58A-C6C9CC95A931 wds:Q57983263-1BCBCB2C-CAC1-4567-B11C-C54F4C9383E4 wds:Q57983263-1D033F7B-A7B8-4035-9140-CFDDA863B1FB wds:Q57983263-224F58F3-1C49-446F-A2AC-DB494986B81F wds:Q57983263-4E8B5453-B825-4063-B89F-F0C9A2237724 wds:Q57983263-545087BD-AA6A-44CD-8A29-B278508D9295 wds:Q57983263-5D7ADA78-627F-4230-999A-844295DDA8FF wds:Q57983263-5ED2C36A-6390-486C-A4B7-1D06D9034A51 wds:Q57983263-777DDAB8-0FE6-4A2F-86D7-D2EA65C8FC25 wds:Q57983263-B2FDB281-0C9D-4097-8F59-80773A32EDC2 wds:Q57983263-D141ECF6-9FF7-4242-90B8-05F8F03D5A20 wds:Q57983263-E0441DB1-D972-439E-9F2E-CC2DBC2E4E57 wds:Q57983263-E240A66D-9C26-476D-BB9E-700D206214B8 wds:Q57983263-E5697A3B-63D0-46D3-88C5-A0333D2E6AA8 wds:Q57983263-F200499F-8DB2-44F1-8177-B904F097729B wds:Q57983263-FF8D1B97-7443-420F-A77E-8E281B8015B4
cites work	Lrrk2 and Lewy body disease. Clinical features of LRRK2-associated Parkinson's disease in central Norway Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family. Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs Common variants of LRRK2 are not associated with sporadic Parkinson's disease Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. Lrrk2 pathogenic substitutions in Parkinson's disease Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations LRRK2 mutations in Parkinson disease Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia Validity and Utility of a LRRK2 G2019S Mutation Test for the Diagnosis of Parkinson's Disease Leucine-rich repeat kinase 2 (LRRK2) mutations in a Swedish Parkinson cohort and a healthy nonagenarian Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease The LRRK2 gene in Parkinson's disease: mutation screening in patients from Germany
author name string	wds:Q57983263-2B343F0D-C5FE-4B01-8D3D-9A77E5AF8C02 wds:Q57983263-CF35FDA4-CB44-479A-A879-6E3098BFC07D
author name string	J O Aasly O A Ross
rdfs:label	LRRK2 and Parkinson?s disease in Norway (en) LRRK2 and Parkinson?s disease in Norway (nl) LRRK2 and Parkinson?s disease in Norway (sq)
skos:prefLabel	LRRK2 and Parkinson?s disease in Norway (en) LRRK2 and Parkinson?s disease in Norway (nl) LRRK2 and Parkinson?s disease in Norway (sq)
name	LRRK2 and Parkinson?s disease in Norway (en) LRRK2 and Parkinson?s disease in Norway (nl) LRRK2 and Parkinson?s disease in Norway (sq)
author	wds:Q57983263-2045E1C5-0D20-45D2-9758-4A60C45753BB wds:Q57983263-71E642F5-FF0F-4BB0-85F7-69F437C8F257 wds:Q57983263-74B8B4FB-C158-4EF1-A021-3B7295148ABE
author	Matthew J. Farrer Kristoffer Haugarvoll Mathias Toft
title	wds:Q57983263-1384470E-2D74-44A6-B3C5-6BDC5F4A5029
title	LRRK2 and Parkinson's disease in Norway (en)
page(s)	wds:Q57983263-076FFDA6-6B69-4C02-9C71-ED70B19F0017
page(s)	72-75
instance of	wds:Q57983263-0C93F37D-6D36-46DA-B21C-308AF54E2276
instance of	scholarly article
main subject	wds:Q57983263-605656E4-E4CF-4370-B56D-A820C0B29A5F
main subject	Parkinson's disease
PubMed ID	wds:Q57983263-C9627CC0-CB28-4148-88AD-64C5EE210386
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17419834
PubMed ID	17419834
published in	wds:Q57983263-36E0478D-8F99-4E83-897D-345D23880281
published in	Acta neurologica Scandinavica. Supplementum
issue	wds:Q57983263-6BDB0BF5-AD38-4D96-A9C6-D42A6F132117
volume	wds:Q57983263-AE7531E0-DFA5-4228-A7AB-D42970E52A24
issue	s187
volume	187
DOI	wds:Q57983263-607F5F80-3A32-4D91-95AB-A8A7F8E6D508
DOI	http://dx.doi.org/10.1111/J.1600-0404.2007.00852.X
DOI	10.1111/J.1600-0404.2007.00852.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57983263
is cites work of	The genetic background of Parkinson's disease: current progress and future prospects Clinical and pathological characteristics of patients with leucine-rich repeat kinase-2 mutations Leucine-Rich Repeat Kinase (LRRK2) Genetics and Parkinson's Disease. LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian population. A Comprehensive Analysis of Population Differences in Variant Distribution in Parkinson's Disease
is cites work of	wds:Q37081406-2F526406-0C5C-4905-9ABE-532E962ECE81 wds:Q34513714-5C6BF1FA-742A-47D2-ADA7-E65CD3A0B1C2 wds:Q38738200-760BD329-D5A1-41DB-93B7-E8F8CBF4A8D5 wds:Q61805965-60AE6503-2FA0-4D8F-98AE-B66C58808E34 wds:Q34177234-7166A834-5813-427A-8669-FD56D6E58F0F

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