Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1. (Human heredity, 1995)

(untitled) - Pericak-Vance, M; Barker, D; Bergoffen, J; Chance, P; Cochrane, S; Dahl, N; Exler, M; Fain, P; Fairweather, N; Fischbeck, K