Publications
Detailed Information
Functional Charaterization of a Novel FGFR2 Mutation, E731K, in Craniosynostosis : 두개골 조기 유합증에서 FGFR2의 Novel Mutation인 E731K의 역할 규명
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- Authors
- Advisor
- 류현모
- Issue Date
- 2009
- Publisher
- 서울대학교 대학원
- Keywords
- 두개골 조기 유합증 ; Craniosynostosis ; Apert syndrome ; Apert syndrome ; FGFR2 ; FGFR2 ; Phosphorylation ; phosphorylation ; Runx2 ; ERK pathway ; Runx2
- Description
- Thesis(masters) --서울대학교 대학원 :치의학과 (구개악안면세포 및 발생생물학전공),2009.2.
- Language
- English
- URI
- http://dcollection.snu.ac.kr:80/jsp/common/DcLoOrgPer.jsp?sItemId=000000037626
https://hdl.handle.net/10371/24627
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