Autonomic and respiratory dysfunction in Charcot–Marie–Tooth disease due to Thr124Met mutation in the myelin protein zero gene
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Clinical Neurology,Neurology,Sensory Systems
Reference33 articles.
1. SPTLC1 is mutated in hereditary sensory neuropathy type I;Bejaoui;Nat Genet,2001
2. Localization of a gene (CMT2A) for autosomal dominant Charcot–Marie–Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity;Ben Othmane;Genomics,1993
3. Neuropathic pain in Charcot–Marie–Tooth disease;Carter;Arch Phys Med Rehabil,1998
4. Axonal phenotype of Charcot–Marie–Tooth disease associated with a mutation in the myelin protein zero gene;Chapon;J Neurol Neurosurg Psychiatry,1999
5. Phrenic nerve conduction study in demyelinating neuropathies and heart surgery;Cruz-Martinez;Clin Neurophysiol,2000
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