Peripheral myelin protein 22 p.Tll8M point mutation in a family with no clinical phenotypes of Charcot-Marie-Tooth disease.
Saved in:
| Title: | Peripheral myelin protein 22 p.Tll8M point mutation in a family with no clinical phenotypes of Charcot-Marie-Tooth disease. |
|---|---|
| Authors: | Sreedevi, N.1 (AUTHOR), Swapna, N.2 (AUTHOR), Maruthy, Santosh1 (AUTHOR), Jayakumar, T.1 (AUTHOR), Meghavathi, H. S.3 (AUTHOR), Sylvester, Charles3 (AUTHOR) charlessylvester29@gmail.com |
| Source: | Journal of Neurosciences in Rural Practice. Jan-Mar2026, Vol. 17 Issue 1, p1-3. 3p. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 09763147 |
|---|---|
| DOI: | 10.25259/JNRP_462_2024 |
