A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion-Reference-Cited by-同舟云学术

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A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion

Published:2004-02-12 Issue:7 Volume:19 Page:812-816
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Dogu Okan,Johnson Janel,Hernandez Dena,Hanson Melissa,Hardy John,Apaydin Hulya,Özekmekçi Sibel,Sevim Serhan,Gwinn-Hardy Katrina,Singleton Andrew

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference20 articles.

1. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism;Kitada;Nature,1998

2. Paralysis agitans of early onset with marked diurnal fluctuation of symptoms;Yamamura;Neurology,1973

3. Localization of a gene for an autosomal recessive form of juvenile parkinsonism to chromosome 6q25.2-27;Matsumine;Am J Hum Genet,1997

4. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe;Abbas;Hum Mol Genet,1999

5. Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism;Lucking;Lancet,1998

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pain in monogenic Parkinson’s disease: a comprehensive review;Frontiers in Neurology;2023-10-30

2. PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson’s disease in Ireland;Irish Journal of Medical Science (1971 -);2021-03-22

3. Twenty years since the discovery of the parkin gene;Journal of Neural Transmission;2017-06-15

4. Nonmotor Signs in Genetic Forms of Parkinson's Disease;INT REV NEUROBIOL;2017

5. Nonmotor Signs in Genetic Forms of Parkinson's Disease;International Review of Neurobiology;2017

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