A Unique Point Mutation in the PMP22 Gene Is Associated with Charcot-Marie-Tooth Disease and Deafness

Margaret J. Kovach(Southern Illinois University School of Medicine), Jing‐Ping Lin(National Institutes of Health), Simeon A. Boyadjiev(Johns Hopkins University), Kathleen C. M. Campbell(Southern Illinois University School of Medicine), Larry Mazzeo(Southern Illinois University School of Medicine), Kristin Herman, Lisa A. Rimer, William E. Frank(Michigan State Police), Barbara Llewellyn(Michigan State Police), Ethylin Wang Jabs(Johns Hopkins University), David A. Gelber(Southern Illinois University School of Medicine), Virginia Kimonis
The American Journal of Human Genetics
June 1, 1999
Cited by 83Open Access
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