Novel genetic linkage of rat <it>Sp6</it> mutation to Amelogenesis imperfecta
<p><b>Abstract</b></p> <p><b>Background</b></p> <p>Amelogenesis imperfecta (AI) is an inherited disorder characterized by abnormal formation of tooth enamel. Although several genes responsible for AI have been reported, not all causative genes fo...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2012-06-01
|
Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | http://www.ojrd.com/content/7/1/34 |