Hereditary Motor and Sensory Neuropathy IIB

Open Access

|Feb 1997

Elliott JL Kwon JM Goodfellow PJ Yee W-C Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristics Neurology 1997 Jan 48 1 23 28 10.1212/WNL.48.1.23 9008488
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Marrosu MG Vaccargiu S Marrosu G Vannelli A Cianchetti C Muntoni F A novel point mutation in the peripheral myelin protein 22 (PMP22) gene associated with Charcot-Marie-Tooth disease type 1A Neurology 1997 Feb 48 2 489 493 10.1212/WNL.48.2.489 9040744
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Language: English

Page range: 13 - 14

Published on: Feb 1, 1997

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

© 1997 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.