The American Journal of Human Genetics
Volume 64, Issue 6, June 1999, Pages 1580-1593
A Unique Point Mutation in the PMP22 Gene Is Associated with Charcot-Marie-Tooth Disease and Deafness
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Charcot-Marie-Tooth Disease (CMT)
Deafness
PMP22 mutation
Anticipation
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Copyright © 1999 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.