Variable phenotypic expression in families with early-onset Parkinsonism due to PRKN mutations

被引：5

作者：

Karkheiran, Siamak ^{[1
]}

Krebs, Catharine E. ^{[2
]}

Darvish, Hossein ^{[3
]}

Asadian, Mojgan ^{[4
]}

Shahidi, Gholam Ali ^{[5
]}

Paisan-Ruiz, Coro ^{[2
,6
,7
,8
,9
]}

机构：

[1] Univ Tehran Med Sci, Hazrat Rasool Hosp, Movement Disorders Clin, Tehran, Iran

[2] Icahn Sch Med Mt Sinai, Dept Neurol, New York, NY 10029 USA

[3] Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran

[4] Isfahan Steel Co, Esfahan, Iran

[5] Univ Tehran Med Sci, Hazrat Rasool Hosp, Dept Neurol, Tehran, Iran

[6] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA

[7] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA

[8] Icahn Sch Med Mt Sinai, Friedman Brain & Mindich Child Hlth Inst, New York, NY 10029 USA

[9] Icahn Sch Med Mt Sinai, Friedman Brain & Mindich Child Dev Inst, New York, NY 10029 USA

来源：

JOURNAL OF NEUROLOGY | 2014年 / 261卷 / 06期

关键词：

DISEASE; DIAGNOSIS; GENOTYPE; PD;

D O I：

10.1007/s00415-014-7360-5

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：1223 / 1226

页数：4

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