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                                       Details for article 7 of 21 found articles
 
 
  Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination
 
 
Title: Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination
Author: Warner, Laura E
Hilz, Max J
Appel, Stanley H
Killian, James M
Kolodny, Edwin H
Karpati, George
Carpenter, Stirling
Watters, Gordon V
Wheeler, Calvin
Witt, David
Bodell, Adria
Nelis, Eva
Van Broeckhoven, Christine
Lupski, James R
Appeared in: Neuron
Paging: Volume 17 (1996) nr. 3 pages 10 p.
Year: 1996
Contents:
Publisher: Cell Press
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 7 of 21 found articles
 
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