(Q53209404)

12 May 2018

title

LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation. (English)

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Jordi Pérez-Tur

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Pau Pastor

object named as

Pau Pastor

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Francesc Valldeoriola

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object named as

Francesc Valldeoriola

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Eduardo Tolosa

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Owen A Ross

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author name string

Oswaldo Lorenzo-Betancor

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Lluís Samaranch

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Elena Lorenzo

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Jaione Irigoyen

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Carles Gaig

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María A Pastor

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Alexandra I Soto-Ortolaza

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María C Rodríguez-Oroz

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María J Martí

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María R Luquin

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Juan A Burguera

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José A Obeso

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language of work or name

English

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publication date

28 October 2011

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12 May 2018

published in

Movement Disorders

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volume

27

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issue

1

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page(s)

146-151

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Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism

cites work

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Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

21 January 2018

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Pathogenic mutations in Parkinson disease

21 January 2018

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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

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LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance

21 January 2018

1 reference

Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease

21 January 2018

1 reference

An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.

21 January 2018

1 reference

LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicity.

21 January 2018

1 reference

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

21 January 2018

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Clinical features of LRRK2 parkinsonism

21 January 2018

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Accuracy of family history data on Parkinson's disease

21 January 2018

1 reference

Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP

21 January 2018

1 reference

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

21 January 2018

1 reference

Roc, a Ras/GTPase domain in complex proteins

21 January 2018

1 reference

GTP binding is essential to the protein kinase activity of LRRK2, a causative gene product for familial Parkinson's disease

21 January 2018

1 reference

Structure of the ROC domain from the Parkinson's disease-associated leucine-rich repeat kinase 2 reveals a dimeric GTPase

21 January 2018

1 reference

Insight into the mode of action of the LRRK2 Y1699C pathogenic mutant

21 January 2018

1 reference

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

21 January 2018

1 reference

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

21 January 2018

1 reference

Genetic screening of the G2019S mutation of the LRRK2 gene in Southwest European, North African, and Sephardic Jewish subjects

21 January 2018

1 reference

The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula

21 January 2018

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LINGO1 gene analysis in Parkinson's disease phenotypes.

21 January 2018

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Globus pallidus dopamine and Parkinson motor subtypes: clinical and brain biochemical correlation

21 January 2018

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A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism

21 January 2018

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Lrrk2 pathogenic substitutions in Parkinson's disease

21 January 2018

1 reference

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

21 January 2018

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A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/MDS.23968

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12 May 2018

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12 May 2018