A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency
| Description | |
| Auteurs | Nicolino M, Claiborn KC, Senee V, Boland A, Stoffers DA and Julier C |
| Revue | |
| Année | 2 010 |
| Service | |
| Institut | |
| Laboratoire | |
| Date de création | 06/01/2017 |
| Facteur Impact | |