Novel frameshift variant of WNT10A in a Japanese patient with hypodontia
Abstract Congenital tooth agenesis is caused by the impairment of crucial genes related to tooth development, such as Wnt signaling pathway genes. Here, we investigated the genetic causes of sporadic congenital tooth agenesis. Exome sequencing, followed by Sanger sequencing, identified a novel singl...
Saved in:
Main Authors: | , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2024-01-01
|
Series: | Human Genome Variation |
Online Access: | https://doi.org/10.1038/s41439-023-00259-4 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|