Functional analysis of RUNX2 mutations in cleidocranial...

Blood Cells, Molecules, and Diseases 2003 Vol. 30; Iss. 2

Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype–phenotype correlations

Taketoshi Yoshida, Hirokazu Kanegane, Motomi Osato, Masatoshi Yanagida, Toshio Miyawaki, Yoshiaki Ito, Katsuya Shigesada
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Volume:
30
Year:
2003
Language:
english
DOI:
10.1016/s1079-9796(03)00020-2
File:
PDF, 377 KB
english, 2003
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