Work

Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype

Year: 2005

Type: article

Source: Journal of Cellular Physiology

DOI: 10.1002/jcp.20552

Authors: Hyo‐Jin Kim, Soon‐Hyeun Nam, Hyun‐Jung Kim, Hyo‐Sang Park, Hyun‐Mo Ryoo, Shin‐Yoon Kim, Tae‐Joon Cho, Seung‐Gon Kim, Suk‐Chul Bae, In‐San Kim, Janet L. Stein, Andre J. van Wijnen, Gary S. Stein, Jane B. Lian, Je‐Yong Choi

Institutions: Kyungpook National University Hospital, Kyungpook National University, Hallym University, Hallym University Sacred Heart Hospital, Seoul National University, Chungbuk National University, University of Massachusetts Chan Medical School

Language: English

Topic: dental development and anomalies

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institute of Dental and Craniofacial Research

Awards: G1648492971, Molecular Control of Bone Formation, G3112959244, Program Project Grant: Bone Cell Structue and Gene Expression, G57866040, Control of Osteoblast Proliferation and Differentiation

OpenAlex ID: W2099188693

FWCI: 1.385

Cites: 38

Cited by: 52

Related to: 10