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공공누리This item is licensed Korea Open Government License

Title
전장유전체 기반 noncoding mutation 위험도 예측 기술 개발 및 한국인 자폐성 범주장애 유전연관성 규명 연구
Alternative Title
Whole genome sequencing-based prediction of risk noncoding mutations and elucidation of genetic association in Korean patients with autism spectrum disorder
Author(s)
김일빈고인경
Publisher
한국과학기술정보연구원
Publication Year
2022
Keyword
자폐범주성장애; 비전사 변이; 임상코호트; 유전 연관성; 유전체분석
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Appears in Collections:
7. KISTI 연구성과 > 연구보고서 > 2022
Type
Report
URI
https://repository.kisti.re.kr/handle/10580/18725
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