Pantothenate Kinase-Associated Neurodegeneration: Clinical Description of 10 Patients and Identification of New Mutations

被引：6

作者：

Assami, Salima ^{[1
,2
]}

Azzedine, Hamid ^{[3
,4
]}

Nouioua, Sonia ^{[1
,2
]}

Mundwiller, Emeline ^{[3
,4
]}

Mahoui, Soulaiman ^{[1
,2
]}

Makri, Samira ^{[5
]}

Djemai, Meriam ^{[6
]}

Grid, Djamel ^{[7
]}

Brice, Alexis ^{[3
,4
,8
]}

Hamadouche, Tarik ^{[9
]}

Stevanin, Giovanni ^{[3
,4
,8
,10
]}

Tazir, Meriem ^{[1
,2
]}

机构：

[1] Univ Alger, Dept Neurol, CHU Mustapha Bacha, Algiers, Algeria

[2] Univ Alger, Neurosci Lab, Algiers, Algeria

[3] INSERM, U975, Paris, France

[4] Univ Paris 06, UMR S975, CNRS 7225, Ctr Rech,Hop Pitie Salpetriere,Inst Cerveau & Moe, Paris, France

[5] EHS Ali Ait Idir, Algiers, Algeria

[6] CHU Bab el Oued, Serv Neurol, Algiers, Algeria

[7] Genethon, Paris, France

[8] Hop La Pitie Salpetriere, APHP, Dept Genet & Cytogenet, Paris, France

[9] Univ Mhamed Bougara, Mol Biol Lab, Boumerdes, Algeria

[10] Ecole Prat Hautes Etud, Paris, France

来源：

MOVEMENT DISORDERS | 2011年 / 26卷 / 09期

关键词：

HALLERVORDEN-SPATZ-SYNDROME; TRIPLE HETEROZYGOSITY;

D O I：

10.1002/mds.23648

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：1777 / 1779

页数：3

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