Literature DB >> 18973067

Spinocerebellar ataxia type 12 was not found in Korean Parkinsonian patients.

Jin Whan Cho1, Sung Yeon Kim, Sung Sup Park, Beom S Jeon.   

Abstract

BACKGROUND: Parkinsonism (PD) is occasionally seen in several types of spinocerebellar ataxia (SCA). Mutations in SCA gene have been reported in the patients of parkinsonism without ataxia.
METHODS: We examined spinocerebellar ataxia type 12 mutation in 877 PD and 199 multiple system atrophy (MSA) patients. RESULTS AND
CONCLUSIONS: No patients showed abnormal SCA12 expansion. It suggests that PD and MSA are not associated with SCA12 and it is not necessary to screen SCA12 in PD and MSA patients.

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Year:  2008        PMID: 18973067     DOI: 10.1017/s0317167100009161

Source DB:  PubMed          Journal:  Can J Neurol Sci        ISSN: 0317-1671            Impact factor:   2.104


  2 in total

1.  Exploration of CAG triplet repeat in nontranslated region of SCA12 gene.

Authors:  Waseem Gul Lone; Imran Ali Khan; Subhadra Poornima; Noor Ahmad Shaik; Angmuthu Kanikannan Meena; Kaipa Prabhakar Rao; Qurratulain Hasan
Journal:  J Genet       Date:  2016-06       Impact factor: 1.166

2.  Genetic players in multiple system atrophy: unfolding the nature of the beast.

Authors:  Sylvia Stemberger; Sonja W Scholz; Andrew B Singleton; Gregor K Wenning
Journal:  Neurobiol Aging       Date:  2011-05-24       Impact factor: 4.673

  2 in total

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