The role of ZFYVE27/protrudin in hereditary spastic paraplegia

被引：23

作者：

Martignoni, Monica ^{[1
]}

Riano, Elena

Rugarli, Elena I. ^{[2
]}

机构：

[1] Ist Neurol C Besta, Div Biochem & Genet, I-20126 Milan, Italy

[2] Univ Milano Bicocca, Dept Neurosci & Med Biotechnol, I-20052 Milan, Italy

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 2008年 / 83卷 / 01期

关键词：

D O I：

10.1016/j.ajhg.2008.05.014

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：127 / 128

页数：2

共 4 条

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[2] Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia [J].

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Heilig, R ;

Weissenbach, J .

NATURE GENETICS, 1999, 23 (03) :296-303

[3] ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia [J].

Mannan, Ashraf U. ;

Krawen, Philip ;

Sauter, Simone M. ;

Boehm, Johann ;

Chronowska, Agnieszka ;

Paulus, Walter ;

Neesen, Juergen ;

Engel, Wolfgang .

AMERICAN JOURNAL OF HUMAN GENETICS, 2006, 79 (02) :351-357

[4] Protrudin induces neurite formation by directional membrane trafficking [J].

Shirane, Michiko ;

Nakayama, Keiichi I. .

SCIENCE, 2006, 314 (5800) :818-821

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