About: Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

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About: Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations Goto Sponge NotDistinct Permalink

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scientific article published on July 2009

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2009 (ast) наукова стаття, опублікована в липні 2009 (uk) مقالة علمية نشرت في يوليو 2009 (ar) scientific article published on July 2009 (en)
publication date	wds:Q37273558-24F18962-39C8-4691-8BCB-AA499088E81F
publication date	2009-07-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37273558-1322F952-1CFF-4C3C-A9E8-4F66E6335AAC
language of work or name	English
cites work	wds:Q37273558-09155DF5-2FFC-44EB-90B8-B859AC50D31C wds:Q37273558-16EFBE92-D9D0-4EB3-9AB4-81948F77639C wds:Q37273558-190985EF-E988-4FB9-9150-072881CFE764 wds:Q37273558-1B90FAF6-3B50-49AB-8EF8-367570DB2055 wds:Q37273558-2043DBCE-1C2D-4519-BF79-E9813EBD1ACC wds:Q37273558-266D2449-3021-4A25-8EB5-3593224D2E7E wds:Q37273558-30AB1988-1B98-48BF-83B3-CCC60109F588 wds:Q37273558-4820F9DC-12F9-448D-BA76-3919D897D965 wds:Q37273558-55159280-7189-4215-9F81-866248B4D76D wds:Q37273558-578CF46C-6C64-4FB6-A8A1-E732C23F7FDA wds:Q37273558-57CA7FB3-C4E3-465D-9C9A-BC581D547A98 wds:Q37273558-5B65B9A9-CC22-48FA-A05A-92D0405491EB wds:Q37273558-5D88DA10-DA4B-4A81-A51B-155C9C1A657E wds:Q37273558-5F09832B-61C0-4C6D-806B-B30E5149BC88 wds:Q37273558-675EDE87-111F-471A-AE88-CB78AD3545F7 wds:Q37273558-6895A56F-A917-4510-99F9-35535FD34A61 wds:Q37273558-726A20F8-ABAB-44A7-92AC-F77DF6B842F9 wds:Q37273558-7D090316-656A-40B5-8CAA-B84E33306F9C wds:Q37273558-7D17C159-72E4-495C-9354-E163D86399A3 wds:Q37273558-815CF391-D640-4DF0-97EE-96469DE3D936 wds:Q37273558-972472B2-97F8-4512-83F8-175B2F1EB027 wds:Q37273558-9967CC1C-BB0A-482C-856C-BBAA336BF64B wds:Q37273558-AA1D0D26-01BF-4775-A342-47F7EDC1C657 wds:Q37273558-BC7F6C8C-A06E-45EC-A8DE-E094D245B59E wds:Q37273558-CA32BEDF-710C-4410-8509-3BD6F598039B wds:Q37273558-E27F854C-E35D-4D5E-863C-F346BD45D050 wds:Q37273558-FD570552-59A5-4BAE-8BA1-9C71B149714C
cites work	The association between quantitative measures of dementia and of senile change in the cerebral grey matter of elderly subjects. 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 Association between early-onset Parkinson's disease and mutations in the parkin gene Genomewide association study for susceptibility genes contributing to familial Parkinson disease Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease Development and validation of a geriatric depression screening scale: a preliminary report Parkinsonism: onset, progression, and mortality Lewy bodies and parkinsonism in families with parkin mutations Genetics of Parkinson disease Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism “Mini-mental state” Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease Complex relationship between Parkin mutations and Parkinson disease Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype. Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro Heterozygousparkinpoint mutations are as common in control subjects as in Parkinson's patients Distribution, type, and origin of Parkin mutations: review and case studies Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations Role of parkin mutations in 111 community-based patients with early-onset parkinsonism Clinical correlates of depressive symptoms in familial Parkinson's disease Mutations in DJ-1 are rare in familial Parkinson disease Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8. wd:Q64862721
author name string	wds:Q37273558-12DE0B31-B2F7-48F9-8AAF-FC8BC4010D30 wds:Q37273558-340D04AB-B6FB-47D0-BF56-AE95299C9EE7 wds:Q37273558-4713C04D-0AD8-4147-84F9-DD59774A3E73 wds:Q37273558-54D8ADE5-1B14-4283-B604-0ECAC920911E wds:Q37273558-58A2D110-714C-4FD2-9D17-BC791E0B0D87 wds:Q37273558-B3C46B84-FE17-41FB-A14B-81FD848FDED3 wds:Q37273558-BFE5ACEA-9725-443E-9B56-0212DDF680B6 wds:Q37273558-CEB68A2C-6631-4856-A0A6-9CE0B2967F56 wds:Q37273558-F2F66EB8-7409-46C8-895B-014706E85740
author name string	T Foroud M W Pauciulo W C Nichols A Rudolph C A Halter D K Kissell K S Marder Parkinson Study Group-PROGENI Investigators R F Pfeiffer
rdfs:label	Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations (en) Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations (ast) Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations. (nl)
skos:prefLabel	Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations (en) Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations (ast) Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations. (nl)
name	Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations (en)

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