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Biochemical Genetics

Volumn 46, Issue 11-12, 2008, Pages 702-707

A novel RUNX2 mutation in cleidocranial dysplasia patients

(6) Xuan, Dongying a Li, Shi b Zhang, Xiong a Lin, Lixin a Wang, Chunxian a Zhang, Jincai a

a SOUTHERN MEDICAL UNIVERSITY (China)

b FOURTH MILITARY MEDICAL UNIVERSITY (China)

Author keywords

Cleidocranial dysplasia; Mutation; RUNX2; Subcellular localization

Indexed keywords

TRANSCRIPTION FACTOR RUNX2;

ARTICLE; CHINA; CLEIDOCRANIAL DYSPLASIA; CONTROLLED STUDY; GENE EXPRESSION; GENE IDENTIFICATION; GENE LOCATION; GENE MUTATION; GENETIC ANALYSIS; HUMAN;

ANIMALS; BASE SEQUENCE; CHINA; CLEIDOCRANIAL DYSPLASIA; CORE BINDING FACTOR ALPHA 1 SUBUNIT; DNA MUTATIONAL ANALYSIS; FAMILY; HUMANS; LUNG; MICE; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; NIH 3T3 CELLS; PROTEIN TRANSPORT; SEQUENCE ANALYSIS;

EID: 55549121197 PISSN: 00062928 EISSN: None Source Type: Journal
DOI: 10.1007/s10528-008-9184-4 Document Type: Article

Times cited : (7)

References (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.