Inherited neuropathies and deafness caused by a PMP22 point mutation: a case report and a review of the literature.
Saved in:
| Title: | Inherited neuropathies and deafness caused by a PMP22 point mutation: a case report and a review of the literature. |
|---|---|
| Authors: | Luigetti, Marco, Zollino, Marcella, Conti, Guido, Romano, Angela, Sabatelli, Mario |
| Source: | Neurological Sciences. Sep2013, Vol. 34 Issue 9, p1705-1707. 3p. |
| Subjects: | Neuropathy, Genetics of deafness, Point mutation (Biology), Neuroanatomy, Biopsy, Myelin proteins, Charcot-Marie-Tooth disease, Genetics |
| Database: | Psychology and Behavioral Sciences Collection |
Be the first to leave a comment!
