Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy

被引：69

作者：

De Marco, Elvira V. ^{[2
]}

Annesi, Grazia ^{[2
]}

Tarantino, Patrizia ^{[2
]}

Rocca, Francesca E. ^{[2
]}

Provenzano, Giovanni ^{[2
]}

Civitelli, Donatella ^{[2
]}

Candiano, Innocenza C. Ciro ^{[2
]}

Annesi, Ferdinanda ^{[2
]}

Carrideo, Sara ^{[2
]}

Condino, Francesca ^{[2
]}

Nicoletti, Giuseppe ^{[1
,2
]}

Messina, Demetrio ^{[1
,2
]}

Novellino, Fabiana ^{[1
]}

Morelli, Maurizio ^{[1
]}

Quattrone, Aldo ^{[1
,2
]}

机构：

[1] Magna Graecia Univ Catanzaro, Fac Med, Inst Neurol, I-88100 Catanzaro, Italy

[2] CNR, Inst Neurol Sci, Cosenza, Italy

来源：

MOVEMENT DISORDERS | 2008年 / 23卷 / 03期

关键词：

Parkinson's disease; Gaucher's disease; glucocerebrosidase;

D O I：

10.1002/mds.21892

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Recent studies have reported an association between the glucocerebrosidase (GBA) gene and Parkinson's disease (PD). To elucidate the role of this gene in our population, we screened 395 PD patients and 483 controls from southern Italy for the N370S and the L444P mutations. We found 11 patients (2.8 %) carrying a heterozygous mutant GBA allele, whereas only one control subject (0.2%) had a heterozygous substitution (P = 0.0018). These results strongly suggest that Italian carriers of a GBA mutation have an increased risk of developing PD. (c) 2007 Movement Disorder Society.

引用

页码：460 / 463

页数：4

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