SIBSHIIP LINKAGE STUDY OF NON-MODULATION AND HYPERTENSION

非调节与高血压的 SIBSHIIP 关联研究

• 批准号: 6245922
• 负责人: ROGER R WILLIAMS
• 金额: $ 2.15万
• 依托单位: UNIVERSITY OF UTAH
• 依托单位国家: 美国
• 财政年份: 1997
• 资助国家: 美国
• 起止时间: 1997-03-06 至 1997-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6245922
• 关键词: cardiovascular disorder diagnosis; clinical research; essential hypertension; familial hypertension; family genetics; gene mutation; genetic disorder; genetic markers; human subject; linkage mapping; phenotype; siblings

Mutations at selected candidate gene loci contribute to the development of essential hypertension and/or intermediate phenotypes of essential hypertension. This hypothesis will be tested using the affected sibling pair method.

选定候选基因位点的突变有助于发展 必需的基本高血压和/或中间表型 高血压。 该假设将使用受影响的兄弟姐妹进行检验 配对方法。