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Comment on "compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism".

作者信息

Sironi F, Primignani P, Goldwurm S

出版信息

Parkinsonism Relat Disord. 2010 Jun;16(5):360-1; author reply 362-3. doi: 10.1016/j.parkreldis.2010.02.005. Epub 2010 Mar 12.

DOI:10.1016/j.parkreldis.2010.02.005

PMID:20227322

Abstract

摘要

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Comment on "compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism".

Parkinsonism Relat Disord. 2010 Jun;16(5):360-1; author reply 362-3. doi: 10.1016/j.parkreldis.2010.02.005. Epub 2010 Mar 12.

Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism.

Parkinsonism Relat Disord. 2009 May;15(4):324-6. doi: 10.1016/j.parkreldis.2008.07.001. Epub 2008 Aug 22.

REM sleep behavior disorder in patients with DJ-1 mutations and parkinsonism-dementia-ALS complex.

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Mutations in DJ-1 are rare in familial Parkinson disease.

Neurosci Lett. 2006 Nov 20;408(3):209-13. doi: 10.1016/j.neulet.2006.09.003. Epub 2006 Sep 25.

Juvenile parkinsonism.

Eur J Paediatr Neurol. 2009 May;13(3):290-2. doi: 10.1016/j.ejpn.2008.04.010. Epub 2008 Jun 20.

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[DJ-1 gene rearrangement mutation in patients with autosomal recessive early-onset parkinsonism using real-time PCR].

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2010 May;35(5):438-44. doi: 10.3969/j.issn.1672-7347.2010.05.006.

Clinical genetics of Parkinson's disease and related disorders.

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Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism.

Neurology. 2003 Nov 25;61(10):1429-31. doi: 10.1212/01.wnl.0000094121.48373.fd.

DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function.

J Med Genet. 2004 Mar;41(3):e22. doi: 10.1136/jmg.2003.011106.

引用本文的文献

DJ1 analysis in a large cohort of Italian early onset Parkinson Disease patients.

Neurosci Lett. 2013 Dec 17;557 Pt B(PB):165-70. doi: 10.1016/j.neulet.2013.10.048. Epub 2013 Oct 28.

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Comment on "compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism".

Parkinsonism Relat Disord. 2010 Jun;16(5):360-1; author reply 362-3. doi: 10.1016/j.parkreldis.2010.02.005. Epub 2010 Mar 12.

Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism.

Parkinsonism Relat Disord. 2009 May;15(4):324-6. doi: 10.1016/j.parkreldis.2008.07.001. Epub 2008 Aug 22.

REM sleep behavior disorder in patients with DJ-1 mutations and parkinsonism-dementia-ALS complex.

Mov Disord. 2009 Jul 30;24(10):1555-6. doi: 10.1002/mds.22629.

Mutations in DJ-1 are rare in familial Parkinson disease.

Neurosci Lett. 2006 Nov 20;408(3):209-13. doi: 10.1016/j.neulet.2006.09.003. Epub 2006 Sep 25.

Juvenile parkinsonism.

Eur J Paediatr Neurol. 2009 May;13(3):290-2. doi: 10.1016/j.ejpn.2008.04.010. Epub 2008 Jun 20.

DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.

Ann Neurol. 2005 Nov;58(5):803-7. doi: 10.1002/ana.20666.

[DJ-1 gene rearrangement mutation in patients with autosomal recessive early-onset parkinsonism using real-time PCR].

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2010 May;35(5):438-44. doi: 10.3969/j.issn.1672-7347.2010.05.006.

Clinical genetics of Parkinson's disease and related disorders.

Parkinsonism Relat Disord. 2007;13 Suppl 3:S229-32. doi: 10.1016/S1353-8020(08)70007-5.

Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism.

Neurology. 2003 Nov 25;61(10):1429-31. doi: 10.1212/01.wnl.0000094121.48373.fd.

DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function.

J Med Genet. 2004 Mar;41(3):e22. doi: 10.1136/jmg.2003.011106.

引用本文的文献

DJ1 analysis in a large cohort of Italian early onset Parkinson Disease patients.

Neurosci Lett. 2013 Dec 17;557 Pt B(PB):165-70. doi: 10.1016/j.neulet.2013.10.048. Epub 2013 Oct 28.

Comment on "compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism".

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