在患有帕金森病的法国家庭中复制的VPS35突变的鉴定。 - Suppr

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Identification of VPS35 mutations replicated in French families with Parkinson disease.

作者信息

Lesage S, Condroyer C, Klebe S, Honoré A, Tison F, Brefel-Courbon C, Dürr A, Brice A

机构信息

Centre de Recherche de l’Institut du Cerveau et de la Moelle épinière, Toulouse, France.

出版信息

Neurology. 2012 May 1;78(18):1449-50. doi: 10.1212/WNL.0b013e318253d5f2. Epub 2012 Apr 18.

DOI:10.1212/WNL.0b013e318253d5f2

PMID:22517097

Abstract

摘要

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相似文献

Identification of VPS35 mutations replicated in French families with Parkinson disease.

Neurology. 2012 May 1;78(18):1449-50. doi: 10.1212/WNL.0b013e318253d5f2. Epub 2012 Apr 18.

The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease.

Mov Disord. 2012 May;27(6):800-1. doi: 10.1002/mds.24927. Epub 2012 Jan 25.

Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease.

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Neurology. 2009 Jun 2;72(22):1882-3. doi: 10.1212/WNL.0b013e3181a81678. Epub 2009 Apr 22.

[How about the uncertainty in the haplotypes in the population-based KORA studies?].

Gesundheitswesen. 2005 Aug;67 Suppl 1:S132-6. doi: 10.1055/s-2005-858253.

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Neurobiol Aging. 2014 Jun;35(6):1512.e1-2. doi: 10.1016/j.neurobiolaging.2013.12.016. Epub 2013 Dec 27.

VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China.

Neurobiol Aging. 2013 Jun;34(6):1709.e7-8. doi: 10.1016/j.neurobiolaging.2012.11.003. Epub 2012 Dec 20.

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Hum Mol Genet. 2022 Mar 3;31(5):705-717. doi: 10.1093/hmg/ddab284.

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Neuroscience. 2019 Mar 1;401:1-10. doi: 10.1016/j.neuroscience.2019.01.006. Epub 2019 Jan 18.

Advances in the Genetics of Parkinson's Disease: A Guide for the Clinician.

Mov Disord Clin Pract. 2014 Apr 10;1(1):3-13. doi: 10.1002/mdc3.12000. eCollection 2014 Apr.