Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia

Published 2015 View Full Article

Authors

Keywords

Journal

AMERICAN JOURNAL OF HUMAN GENETICS

Volume 97, Issue 4, Pages 621-626

Publisher

Elsevier BV

Online

2015-09-18

DOI

10.1016/j.ajhg.2015.08.014

Ask authors/readers for more resources

Protocol

Community support

Reagent

Community support

Reprint

Contact the author

Publish scientific posters with Peeref

Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.

Learn More

Ask a Question. Answer a Question.

Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.

Get Started