Wolfram syndrome with a rare genetic mutation - Case report
oleh: Divya U Caculo, Sowmya Raveendra Murthy, Ankita A Patil, Sneha R Peswani
| Format: | Article |
|---|---|
| Diterbitkan: | Wolters Kluwer Medknow Publications 2022-01-01 |
Deskripsi
Subjek
deafness; genetic analysis; juvenile diabetes mellitus; optic atrophy; wolfram syndrome