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Functional characterization of Connexin43 mutations found in patients presenting with oculodentodigital dysplasia (ODDD)
被引:0
|作者:
Musa, H
Paznekas, W
Shibayama, J
Seki, A
Coombs, W
Taffet, S
Jabs, EW
Delmar, M
机构:
[1] SUNY Upstate Med Univ, Syracuse, NY USA
[2] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
关键词:
D O I:
暂无
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
1710
引用
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页码:309A / 309A
页数:1
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