Parkin mutations are frequent in patients with isolated early‐onset parkinsonism-Reference-Cited by-同舟云学术

Parkin mutations are frequent in patients with isolated early‐onset parkinsonism

Published:2003-06 Issue:6 Volume:126 Page:1271-1278
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Periquet Magali,Latouche Morwena,Lohmann Ebba,Rawal Nina,De Michele Giuseppe,Ricard Sylvain,Teive Hélio,Fraix Valérie,Vidailhet Marie,Nicholl David,Barone Paolo,Wood Nick W.,Raskin Salmo,Deleuze Jean‐François,Agid Yves,Dürr Alexandra,Brice Alexis

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/126/6/1271/9172063/awg136.pdf

Reference35 articles.

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2. Bonifati V, Rizzu P, Van Baren MJ, et al. Mutations in the DJ‐1 gene associated with autosomal recessive early‐onset parkonsonism. Science2002; 299: 256–9.

3. Elbaz A, Grigoletto F, Baldereschi M, Breteler MM, Manubens‐Bertan JM, Lopez‐Pousa S, et al. Familial aggregation of Parkinson’s disease: a population‐based case‐control study in Europe. EUROPARKINSON Study Group. Neurology1999; 52: 1876–82.

4. Farrer M, Gwinn‐Hardy K, Muenter M, DeVreize FW, Crook, R, Perez‐Tur, J, et al. A chromosome 4p haplotype segregating with Parkinson’s disease and postural tremor. Hum Mol Genet1999; 8: 81–5.

5. Farrer M, Chan P, Chen R, Tan L, Lincoln S, Hernandez D, et al. Lewy bodies and parkinsonism in families with parkin mutations. Ann Neurol2001; 50: 293–300.

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