Identification of novel CLN2 mutations shows Canadian specific NCL2 alleles

被引：23

作者：

Ju, W

Zhong, R

Moore, S

Moroziewicz, D

Currie, JR

Parfrey, P

Brown, WT

Zhong, N

机构：

[1] New York State Inst Basic Res Dev Disabil, SCL Mol Neurogenet Diagnost Lab, Staten Isl, NY 10314 USA

[2] New York State Inst Basic Res Dev Disabil, Dept Human Genet, Staten Isl, NY 10314 USA

[3] Suny Downstate Med Ctr, Dept Neurol, Brooklyn, NY 11203 USA

[4] Stuyvesant High Sch, New York, NY USA

[5] Mem Univ Newfoundland, Hlth Sci Ctr, Clin Epidemiol Unit, St Johns, NF, Canada

来源：

JOURNAL OF MEDICAL GENETICS | 2002年 / 39卷 / 11期

关键词：

D O I：

10.1136/jmg.39.11.822

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：822 / 825

页数：4

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