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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-50709

Tomiyasu, A; Nakamura, M; Ichiba, M; Ueno, S; Saiki, S; Morimoto, M; Kobal, J; Kageyama, Y; Inui, T; Wakabayashi, K; Yamada, T; Kanemori, Y; Jung, H H; Tanaka, H; Orimo, S; Afawi, Z; Blatt, I; Aasly, J; Ujike, H; Babovic-Vuksanovic, D; Josephs, K A; Tohge, R; Rodrigues, G R; Düpre, N; Yamada, H; Yokochi, F; Kotschet, K; Takei, T; Rudzińska, M; Szczudlik, A; Penco, S; Fujiwara, M; Tojo, K; Sano, A (2011). Novel pathogenic mutations and copy number variations in the VPS13A gene in patients with chorea-acanthocytosis. American Journal of Medical Genetics. Part B, 156(5):620-631.

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Abstract

Chorea-acanthocytosis (ChAc) is a rare autosomal recessive neurodegenerative disorder caused by loss of function mutations in the vacuolar protein sorting 13 homolog A (VPS13A) gene that encodes chorein. It is characterized by adult-onset chorea, peripheral acanthocytes, and neuropsychiatric symptoms. In the present study, we performed a comprehensive mutation screen, including sequencing and copy number variation (CNV) analysis, of the VPS13A gene in ChAc patients. All 73 exons and flanking regions of VPS13A were sequenced in 35 patients diagnosed with ChAc. To detect CNVs, we also performed real-time quantitative PCR and long-range PCR analyses for the VPS13A gene on patients in whom only a single heterozygous mutation was detected. We identified 36 pathogenic mutations, 20 of which were previously unreported, including two novel CNVs. In addition, we investigated the expression of chorein in 16 patients by Western blotting of erythrocyte ghosts. This demonstrated the complete absence of chorein in patients with pathogenic mutations. This comprehensive screen provides an accurate and useful method for the molecular diagnosis of ChAc.

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > University Hospital Zurich > Clinic for Neurology
DDC:610 Medicine & health
Language:English
Date:2011
Deposited On:07 Nov 2011 10:04
Last Modified:01 Jan 2014 01:06
Publisher:Wiley-Blackwell
ISSN:1552-4841
Publisher DOI:10.1002/ajmg.b.31206
PubMed ID:21598378
Citations:Web of Science®. Times Cited: 10
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Scopus®. Citation Count: 8

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