(Q54543700)

31 May 2018

title

A Korean Parkinson's disease family with the LRRK2 p.Tyr1699Cys mutation showing clinical heterogeneity. (English)

1 reference

31 May 2018

1 reference

5

1 reference

31 May 2018

author name string

Ji Sun Kim

1

1 reference

31 May 2018

Jin Whan Cho

2

1 reference

31 May 2018

Hyeeun Shin

3

1 reference

31 May 2018

Won Yong Lee

4

1 reference

31 May 2018

Ah Ra Cho

6

1 reference

31 May 2018

Hee-Tae Kim

7

1 reference

31 May 2018

language of work or name

English

0 references

publication date

9 December 2011

1 reference

31 May 2018

published in

Movement Disorders

1 reference

31 May 2018

volume

27

1 reference

31 May 2018

issue

2

1 reference

31 May 2018

page(s)

320-324

1 reference

31 May 2018

Complex segregation analysis of Parkinson's disease: The Mayo Clinic Family Study

cites work

1 reference

Parkinson's disease and family history

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

LRRK2 G2019S in the North African population: a review

21 January 2018

1 reference

Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

21 January 2018

1 reference

The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?

21 January 2018

1 reference

LRRK2 G2019S founder haplotype in the Chinese population

21 January 2018

1 reference

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China

21 January 2018

1 reference

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

21 January 2018

1 reference

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

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

1 reference

The metric properties of a novel non-motor symptoms scale for Parkinson's disease: Results from an international pilot study

21 January 2018

1 reference

Quantitation of non-motor symptoms in Parkinson's disease

21 January 2018

1 reference

Identifying the pattern of olfactory deficits in Parkinson disease using the brief smell identification test

21 January 2018

1 reference

Development of the 12-item Cross-Cultural Smell Identification Test (CC-SIT).

21 January 2018

1 reference

Systematic review of levodopa dose equivalency reporting in Parkinson's disease.

21 January 2018

1 reference

Clinical features of LRRK2-associated Parkinson's disease in central Norway

21 January 2018

1 reference

Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease

21 January 2018

1 reference

Clinical genetic analysis of Parkinson's disease in the Contursi kindred

21 January 2018

1 reference

Review: Familial Parkinson's disease--genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease

21 January 2018

1 reference

Clinical, neuropathological and genotypic variability in SNCA A53T familial Parkinson's disease. Variability in familial Parkinson's disease

21 January 2018

1 reference

Clinical and genetic study of familial Parkinson's disease in Tunisia

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.24033

1 reference

31 May 2018

1 reference

31 May 2018