Abstract
Holt-Oram syndrome has been associated with mutations in the T-box transcription factor TBX5, but little is known about the function of this protein or how mutations in it cause disease. A new mouse model of this syndrome will help to answer some of these questions.
| Original language | American English |
|---|---|
| Journal | Nature medicine |
| Volume | 7 |
| State | Published - Jan 1 2001 |
Disciplines
- Developmental Biology
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