Haploinsufficiency of MSX1: a Mechanism for Selective Tooth Agenesis

Previously, we found that the cause of autosomal dominant selective tooth agenesis in one family is a missense mutation resulting in an arginine-to-proline substitution in the homeodomain of MSX1. To determine whether the tooth agenesis phenotype may result from haploinsufficiency or a dominant-nega...

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Detaylı Bibliyografya
Asıl Yazarlar: Hu, Gezhi, Vastardis, Heleni, Bendall, Andrew J., Wang, Zhaoqing, Logan, Malcolm, Zhang, Hailan, Nelson, Craig, Stein, Stacey, Greenfield, Norma, Seidman, Christine E., Seidman, J. G., Abate-Shen, Cory
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Microbiology 1998
Konular:
Transcriptional Regulation
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC109190/
https://ncbi.nlm.nih.gov/pubmed/9742121
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