转甲状腺素
点突变
淀粉样变性
外显子
聚合酶链反应
单链构象多态性
分子生物学
突变
底漆(化妆品)
腕管综合征
医学
病理
淀粉样蛋白(真菌学)
基因
化学
遗传学
生物
外科
有机化学
作者
T. Murakami,Shinya Tachibana,Yasuhisa Endo,R. Kawai,Mitsuru Hara,Sumio Tanase,M Ando
出处
期刊:Neurology
[Lippincott Williams & Wilkins]
日期:1994-02-01
卷期号:44 (2): 315-315
被引量:54
摘要
We studied two patients from a Japanese family with carpal tunnel syndrome (CTS). The biopsy samples obtained during CTS surgical release revealed deposits of amyloid that stained with antihuman transthyretin (TTR) antiserum. Single-strand conformation polymorphism analysis and sequence analysis of polymerase chain reaction (PCR)-amplified exons of the proband's TTR gene revealed a point mutation resulting in a substitution of histidine for tyrosine at position 114. The mutation was confirmed by PCR-primer-induced restriction analysis. Our findings account for clinical heterogeneity of TTR-derived amyloidosis, and suggest the importance of substitution itself for deposits of amyloid in CTS.
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