Functional analysis of a novel RUNX2 missense mutation found in a family with cleidocranial dysplasia

PUPPIN C

•

PELLIZZARI L

•

FABBRO D

altro

DAMANTE G

2005

journal article

Periodico

JOURNAL OF HUMAN GENETICS

DOI

10.1007/s10038-005-0311-3

WOS

WOS:000233791400013

Archivio

http://hdl.handle.net/11390/877059

info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-28844436016

Diritti

closed access

Soggetti

Web of Science© citazioni

11

Data di acquisizione
Mar 25, 2024

Visualizzazioni

4

Data di acquisizione
Apr 19, 2024