SCA16 is really SCA15

被引：18

作者：

Gardner, R. J. M. ^{[1
]}

机构：

[1] Genet Hlth Serv Victoria, Melbourne, Vic 3052, Australia

来源：

JOURNAL OF MEDICAL GENETICS | 2008年 / 45卷 / 03期

关键词：

D O I：

10.1136/jmg.2007.056341

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：192 / 192

页数：1

共 5 条

[1] Spinocerebellar ataxia type 15 [J].

Gardner, RJM ;

Knight, MA ;

Hara, K ;

Tsuji, S ;

Forrest, SM ;

Storey, E .

CEREBELLUM, 2005, 4 (01) :47-50

[2]

IWAKI A, 2007, J MED GENET

[3] Spinocerebellar ataxia type 15 (SCA15) maps to 3p24.2-3pter:: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant [J].

Knight, MA ;

Kennerson, ML ;

Anney, RJ ;

Matsuura, T ;

Nicholson, GA ;

Salimi-Tari, P ;

Gardner, RJM ;

Storey, E ;

Forrest, SM .

NEUROBIOLOGY OF DISEASE, 2003, 13 (02) :147-157

[4] A new autosomal dominant pure cerebellar ataxia [J].

Storey, E ;

Gardner, RJM ;

Knight, MA ;

Kennerson, ML ;

Tuck, RR ;

Forrest, SM ;

Nicholson, GA .

NEUROLOGY, 2001, 57 (10) :1913-1915

[5] Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans [J].

van de Leemput, Joyce ;

Chandran, Jayanth ;

Knight, Melanie A. ;

Holtzclaw, Lynne A. ;

Scholz, Sonja ;

Cookson, Mark R. ;

Houlden, Henry ;

Gwinn-Hardy, Katrina ;

Fung, Hon-Chung ;

Lin, Xian ;

Hernandez, Dena ;

Simon-Sanchez, Javier ;

Wood, Nick W. ;

Giunti, Paola ;

Rafferty, Ian ;

Hardy, John ;

Storey, Elsdon ;

Gardner, R. J. McKinlay ;

Forrest, Susan M. ;

Fisher, Elizabeth M. C. ;

Russell, James T. ;

Cai, Huaibin ;

Singleton, Andrew B. .

PLOS GENETICS, 2007, 3 (06) :1076-1082

← 1 →