P467: A novel mutation in HSPG2 gene causing Schwartz Jampel syndrome
oleh: Parminder Parminder
| Format: | Article |
|---|---|
| Diterbitkan: | Elsevier 2024-01-01 |
Deskripsi
No description available for this item.
oleh: Parminder Parminder
| Format: | Article |
|---|---|
| Diterbitkan: | Elsevier 2024-01-01 |
No description available for this item.