生物
外显子
遗传学
突变
早老素
基因
疾病
阿尔茨海默病
内科学
医学
作者
Maria Guadalupe Ramírez‐Dueñas,E. Rogaeva,Caridad Leal,Changqing Lin,G. A. Ramirez-Casillas,J. A. Hernandez-Romo,Peter St George‐Hyslop,J M Cantú
出处
期刊:PubMed
[National Institutes of Health]
日期:1998-01-01
卷期号:41 (3): 149-53
被引量:25
摘要
A search for mutations in exons 6, 7, 9 and 12 of the PS1 gene in four Mexican families with Early-Onset (36-40 years) Alzheimer Disease yielded the discovery in one family of a T-->C mismatch in exon 7 which correspond to nucleotide 760 of cDNA, leading to a Leu171Pro mutation. The pedigree analysis and the literature data strongly suggest an etiopathogenic relationship of the mutation with the disorder.
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