Hereditary chin trembling: A new family with exclusion of the chromosome 9q13-q21 locus

被引：19

作者：

Grimes, DA

Han, F

Bulman, D

Nicolson, ML

Suchowersky, O

机构：

[1] Ottawa Hlth Res Inst, Ottawa, ON, Canada

[2] Parkinsons Dis & Movement Disorders Clin, Ottawa, ON, Canada

[3] Univ Calgary, Movement Disorders Clin, Calgary, AB, Canada

来源：

MOVEMENT DISORDERS | 2002年 / 17卷 / 06期

关键词：

hereditary chin trembling; linkage analysis; chromosome; 9q13-21;

D O I：

10.1002/mds.10275

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Hereditary chin trembling is a rare autosomal dominant condition that has been linked to chromosome 9q 13-21 in one kindred. We describe a four-generation family with this condition and, using linkage analysis, have excluded the 9q 1321 region as causing the chin trembling in this family. (C) 2002 Movement Disorder Society.

引用

页码：1390 / 1392

页数：3

共 9 条

[1] Hereditary chin trembling or hereditary chin myoclonus? [J].