Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders (vol 21, pg 5417, 2012)

Peoch Katell; Levavasseur Etienne; Delmont Emilien; De Simone Alfonso; Laffont-Proust Isabelle; Privat Nicolas; Chebaro Yassmine; Chapuis Celine; Bedoucha Pierre; Brandel Jean-Philippe; Laquerriere Annie; Kemeny Jean-Louis; Hauw Jean-Jacques; Borg Michel; Rezaei Human; Derreumaux Philippe; Laplanche Jean-Louis; Haik Stephane

首页> 外文期刊>Human Molecular Genetics >Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders (vol 21, pg 5417, 2012)

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Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders (vol 21, pg 5417, 2012)

机译：ion病毒蛋白第211位残基的取代驱动CJD和GSS综合征之间的转换，这是一种控制遗传性神经退行性疾病的新机制（第21卷，第5417页，2012年）

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《Human Molecular Genetics》 |2014年第8期|共1页
作者
Peoch Katell; Levavasseur Etienne; Delmont Emilien; De Simone Alfonso; Laffont-Proust Isabelle; Privat Nicolas; Chebaro Yassmine; Chapuis Celine; Bedoucha Pierre; Brandel Jean-Philippe; Laquerriere Annie; Kemeny Jean-Louis; Hauw Jean-Jacques; Borg Michel; Rezaei Human; Derreumaux Philippe; Laplanche Jean-Louis; Haik Stephane;
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正文语种 eng
中图分类医学遗传学;
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1. Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders (vol 21, pg 5417, 2012) [J] . Peoch Katell, Levavasseur Etienne, Delmont Emilien, Human Molecular Genetics . 2014,第8期

机译：ion病毒蛋白第211位残基的取代驱动CJD和GSS综合征之间的转换，这是一种控制遗传性神经退行性疾病的新机制（第21卷，第5417页，2012年）
2. Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders [J] . Human Molecular Genetics . 2012,第26期

机译：ion病毒蛋白残基211的取代驱动CJD和GSS综合征之间的转换，这是一种控制遗传性神经退行性疾病的新机制
3. Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders [J] . Katell Peoch123 Etienne Levavasseur3456 Emilien Delmont7 Alfonso De Simone8 Isabelle Laffont-Proust3456 Nicolas Privat3456 Yassmine Chebaro9 Céline Chapuis10 Pierre Bedoucha7 Jean-Philippe Brandel345611 Annie Laquerriere12 Jean-Louis Kemeny13 Jean-Jacques Hauw345614 Michel Borg15 Human Rezaei10 Philippe Derreumaux9 Jean-Louis Laplanche123 and Stéphane Haïk34561114* Human Molecular Genetics . 2012,第26期

机译：ion病毒蛋白残基211的取代驱动CJD和GSS综合征之间的转换，这是一种控制遗传性神经退行性疾病的新机制
4. Absence of disease related prion protein in neurodegenerative disorders presenting with Parkinsons syndrome. [O] . K Jendroska, O Hoffmann, L Schelosky, 1994

机译：帕金森综合症所致的神经退行性疾病中缺乏与疾病相关的病毒蛋白。
5. C-21 * Neuropsychological Evaluation in the Differential Diagnosis of Neurodegenerative vs. Nonneurodegenerative Disorders: A Case Study of Capgras Syndrome [O] . K. Szczepkowski, C. Lewandowski, K. Callahan, 2014

机译：C-21 *神经变性与非通量疾病的鉴别诊断中的神经心理学评价：Capgras综合征的案例研究

Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders (vol 21, pg 5417, 2012)

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