Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease-Reference-Cited by-同舟云学术

Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease

Published:2015-03-20 Issue:3 Volume:16 Page:241-242
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Chao Yin Xia,Ng Ebonne Yulin,Foo Jia Nee,Liu Jianjun,Zhao Yi,Tan Eng-King

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-015-0443-3.pdf

Reference5 articles.

1. Tan EK, Lee SS, Fook-Chong S, Lum SY (2008) Evidence of increased odds of essential tremor in Parkinson’s disease. Mov Disord 23(7):993–997

2. Vilariño-Güell C, Wider C, Ross OA, Jasinska-Myga B, Kachergus J et al (2010) LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease. Neurogenetics 11(4):401–408

3. Unal Gulsuner H, Gulsuner S, Mercan FN, Onat OE, Walsh T et al (2014) Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease. Proc Natl Acad Sci U S A 111(51):18285–18290

4. Hughes AJ, Daniel SE, Kilford L, Lees AJ (1992) Accuracy of clinical diagnosis of idiopathic Parkinson’s disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 55:181–184

5. Deuschl G, Bain P, Brin M (1998) Consensus statement of the Movement Disorder Society on Tremor. Ad Hoc Scientific Committee. Mov Disord 13(Suppl 3):2–23

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