[Gangliosidosis GM2 type 2 (Sandhoff disease)].
作者信息
Sánchez-Corona J, Vaca G, González-Flores S A, Villar V, Solé M T, Barajas L O, Velázquez R, Valdez-Luviano J, Cantú J M
出版信息
Rev Invest Clin. 1985 Jan-Mar;37(1):43-7.
PMID:4001618
Abstract
摘要
相似文献
1
[Gangliosidosis GM2 type 2 (Sandhoff disease)].[GM2 型神经节苷脂沉积症 2 型（桑德霍夫病）]
Rev Invest Clin. 1985 Jan-Mar;37(1):43-7.
2
Identification of Sandhoff disease in a Thai family: clinical and biochemical characterization.
J Med Assoc Thai. 2010 Sep;93(9):1088-92.
3
Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon.桑德霍夫病：黎巴嫩一种常见的婴儿型GM2神经节苷脂贮积症。
Am J Hum Genet. 1981 Jan;33(1):85-9.
4
[Sandhoff disease].[桑德霍夫病]
An Esp Pediatr. 1984 Nov 15;21(7):688-92.
5
[Sandhoff's and Tay-Sachs disease--based on our own cases].[基于我们自己的病例的桑德霍夫病和泰-萨克斯病]
Klin Oczna. 2004;106(3 Suppl):534-6.
6
[GM2 gangliosidosis--Tay-Sacks disease and Sandhoff's disease].[GM2神经节苷脂沉积症——泰-萨克斯病和桑德霍夫病]
Nihon Rinsho. 1978 May;Suppl:1394-5.
7
[Sandhoff disease or GM2 gangliosidosis, type 2. High frequency of the gene in a native population].
Medicina (B Aires). 1980 Jan-Feb;40(1):55-73.
8
[Detection of homozygotes and heterozygote carriers of GM2-gangliosidosis].[GM2神经节苷脂贮积症纯合子及杂合子携带者的检测]
Genetika. 1986 Aug;22(8):2179-85.
9
High-resolution loading tests in the study of genetic heterogeneity in gangliosidosis fibroblasts.神经节苷脂贮积症成纤维细胞遗传异质性研究中的高分辨率负荷试验
J Inherit Metab Dis. 1994;17(1):104-11. doi: 10.1007/BF00735405.
10
[Genetic deficiencies of beta-N-acetylhexosaminidase A and B: Tay-Sachs and Sandhoff diseases (GM2-gangliosidosis)].β-N-乙酰己糖胺酶A和B的基因缺陷：泰-萨克斯病和桑德霍夫病（GM2神经节苷脂贮积症）
Tanpakushitsu Kakusan Koso. 1988 Apr;33(5):721-7.
Zotero 插件