Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystonia

被引:20
作者
Klein, C
Hedrich, K
Kabakçi, K
Mohrmann, K
Wiegers, K
Landt, O
Hagenah, J
Schwinger, E
Pramstaller, PP
Ozelius, LJ
Gucuyener, K
Aysun, S
Demir, E
机构
[1] Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany
[2] Med Univ Lubeck, Dept Human Genet, D-23538 Lubeck, Germany
[3] TIB MOLBIOL, Berlin, Germany
[4] Reg Gen Hosp, Dept Neurol, Bolzano, Italy
[5] Albert Einstein Coll Med, Bronx, NY 10467 USA
[6] Gazi Univ, Dept Pediat Neurol, Ankara, Turkey
[7] Univ Hacettepe, Dept Pediat Neurol, TR-06100 Ankara, Turkey
关键词
D O I
10.1212/01.WNL.0000035629.04791.3F
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Most cases of dopa-responsive dystonia (DRD) are thought to be caused by mutations in the GCHI gene; however, by sequencing, mutations are found in only 40% to 60%. Recently, a single report identified, via Southern blot analysis, a large genomic GCHI deletion in a "mutation-negative" case. This report describes four families with DRD, two of which carry large deletions, thus confirming that deletions are an important subtype of GCHI mutations. These deletions were detected by quantitative duplex PCR that is amenable to DNA diagnostics.
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页码:1783 / 1786
页数:4
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