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Functional Charaterization of a Novel FGFR2 Mutation, E731K, in Craniosynostosis
두개골 조기 유합증에서 FGFR2의 Novel Mutation인 E731K의 역할 규명

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Authors
박정현
Advisor
류현모
Issue Date
2009
Publisher
서울대학교 대학원
Keywords
두개골 조기 유합증CraniosynostosisApert syndromeApert syndromeFGFR2FGFR2PhosphorylationphosphorylationRunx2ERK pathwayRunx2
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

http://hdl.handle.net/10371/24627
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College of Dentistry/School of Dentistry (치과대학/치의학대학원)Dept. of Dentistry (치의학과)Theses (Master's Degree_치의학과)
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