Inherited neuropathies and deafness caused by a PMP22 point mutation: a case report and a review of the literature.

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Bibliographic Details
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
Description
ISSN:15901874
DOI:10.1007/s10072-012-1277-5