2016•Journal of Oral and Maxillofacial Surgery Medicine and PathologyRequires access

Novel RUNX2/CBFA1 mutation in the runt domain in a Japanese patient with cleidocranial dysplasia

Hiroki Goto, Junichiro Machida, Akio Shibata, Tadashi Tatematsu, Eriko Osumi, Hitoshi Miyachi, Katsu Takahashi, Atsuo Nakayama, Yujiro Higashi, Toru Nagao, Kazuo Shimozato, Yoshihito Tokita

Open publisher page 1 citations

Abstract

This record does not include an abstract. Use the full-text link above if available.

About this research paper

What this paper is about

An abstract is not available in the OpenAlex record for this paper.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Key concepts: Cleidocranial Dysplasia, Haploinsufficiency, RUNX2, Transcription factor, Biology, Osteoblast, Short stature, Dysplasia

Back to paper search Browse research topics Original source

Novel RUNX2/CBFA1 mutation in the runt domain in a Japanese patient with cleidocranial dysplasia — Research Paper | ScholarLens