✦ LIBER ✦

A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease

✍ Scribed by Benoit G. Bruneau; Georges Nemer; Joachim P. Schmitt; Frédéric Charron; Lynda Robitaille; Sophie Caron; David A. Conner; Manfred Gessler; Mona Nemer; Christine E. Seidman; J.G. Seidman

Book ID: 117268876
Publisher: Elsevier Science
Year: 2001
Tongue: English
Weight: 702 KB
Volume: 106
Category: Article
ISSN: 0092-8674
DOI: 10.1016/s0092-8674(01)00493-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Holt-Oram syndrome is caused by mutation

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family: Li, Q.Y. et al. Nat. Genet. 15, 21–29 Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome Basson, C.T. et al. Nat. Genet. 15, 30–35

📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 87 KB