Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease-Reference-Cited by-同舟云学术

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Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease

Published:2005 Issue:1 Volume:133B Page:120-123
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Clarimon Jordi,Johnson Janel,Dogu Okan,Horta Wagner,Khan Naheed,Lees Andrew J.,Hardy John,Singleton Andrew

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Reference14 articles.

1. A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

2. Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer

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

4. Segmental duplications: an 'expanding' role in genomic instability and disease

5. Accuracy in the clinical diagnosis of parkinsonian syndromes.

Cited by 18 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. Genetics of Parkinson’s disease in Brazil: a systematic review of monogenic forms;Arquivos de Neuro-Psiquiatria;2021-07

2. Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel;Frontiers in Neurology;2017-10-31

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

4. Mutation analysis of the PARKIN, PINK1, DJ1, and SNCA genes in Turkish early-onset Parkinson’s patients and genotype-phenotype correlations;Clinical Neurology and Neurosurgery;2016-09

5. Genomic mechanisms underlyingPARK2large deletions identified in a cohort of patients with PD;Neurology Genetics;2016-05-03

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