A novel FUCA1 mutation causing fucosidosis in a Chinese boy

被引:8
作者
Ip, P [1 ]
Goh, W [1 ]
Chan, KW [1 ]
Cheung, PT [1 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Paediat, Hong Kong, Hong Kong, Peoples R China
关键词
D O I
10.1023/A:1020116220624
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report a 6-year-old boy with an intermediate form of fucosidosis.
引用
收藏
页码:415 / 416
页数:2
相关论文
共 3 条
[1]   A fucosidosis patient with relative longevity and a missense mutation in exon 7 of the α-fucosidase gene [J].
Fleming, CJ ;
Sinclair, DU ;
White, EJ ;
Winchester, B ;
Whiteford, ML ;
Connor, JM .
JOURNAL OF INHERITED METABOLIC DISEASE, 1998, 21 (06) :688-689
[2]   A case of chronic infantile type of fucosidosis: clinical and magnetic resonance image findings [J].
Inui, K ;
Akagi, M ;
Nishigaki, T ;
Muramatsu, T ;
Tsukamoto, H ;
Okada, S .
BRAIN & DEVELOPMENT, 2000, 22 (01) :47-49
[3]   Spectrum of mutations in fucosidosis [J].
Willems, PJ ;
Seo, HC ;
Coucke, P ;
Tonlorenzi, R ;
O'Brien, JS .
EUROPEAN JOURNAL OF HUMAN GENETICS, 1999, 7 (01) :60-67