Gly(247) → Asp proenkephalin A mutation is rare in schizophrenia populations

AMERICAN JOURNAL OF MEDICAL GENETICS(1997)

引用 5|浏览4
暂无评分
摘要
Schizophrenia is a complex and severe disorder of unknown cause and pathophysiology, In previous work examining an opioid hypothesis for schizophrenia, we identified a missense mutation (Gly(247) --> Asp) in the proenkephalin A gene of one African-American patient, In the current study involving an extended set of African-American and other patients, we sought to identify additional mutant alleles and to determine the distribution of these alleles among several racial groups, However, the Gly(247) --> Asp allele was not detected in any of 116 African-American (67 cases, 49 controls), 659 Caucasian, 1 Hispanic, 4 Asian, and 7 Native American individuals. Therefore, it appears that this mutation is a rare event of unknown clinical significance, (C) 1997 Wiley-Liss, Inc.
更多
查看译文
关键词
schizophrenia,genetics,proenkephalin
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要