Congenital hypomyelinating neuropathy due to the association of a truncating mutation in PMP22 with the classical HNPP deletion. Jouaud M, Gonnaud P-M, Richard L, Latour P, Ollagnon-Roman E, Sturtz F, Mathis S, Magy L, Vallat J-M Neuromuscul Disord. 2016 Apr-May; 26(4-5):316-21. Epub 2016 Apr 05. PMID: 27067623. Abstract CommentRecommendBookmarkWatch