一个 de novo Alu 插入导致神经纤维素瘤 1 型
M R Wallace1, L B Andersen, A M Saulino
1Howard Hughes Medical Institute, University of Michigan, Ann Arbor 48109-0650.
Nature
|October 31, 1991
概括
1型神经纤维素瘤病 (NF1) 是由NF1基因的独特突变引起的. 一种新的de novo Alu插入通过改变基因拼接和阅读框架导致NF1,揭示了一个新的突变机制.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 人类疾病 人类疾病
背景情况:
- 神经纤维素瘤类型1 (NF1) 是一种常见的遗传性疾病.
- 它呈现出诸如神经纤维瘤和咖啡牛奶斑等可变症状.
- 位于第17染色体上的NF1基因最近被确定.
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