MESP1 Mutations in Patients with Congenital Heart Defects
Identifying the genetic etiology of congenital heart disease (CHD) has been challenging despite being one of the most common congenital malformations in humans. We previously identified a microdeletion in a patient with a ventricular septal defect containing over 40 genes including MESP1 (mesoderm p...
Saved in:
| Main Authors: | , , , |
|---|---|
| Format: | Text |
| Language: | English |
| Published: |
2016
|
| Subjects: | |
| Online Access: | https://pmc.ncbi.nlm.nih.gov/articles/PMC4762608/ https://pubmed.ncbi.nlm.nih.gov/26694203 http://dx.doi.org/10.1002/humu.22947 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|