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Editorial
. 2002 Dec 24;59(12):1835-6.
doi: 10.1212/wnl.59.12.1835.

GDAP1 mutations in CMT4: axonal and demyelinating phenotypes?: The exception "proves the rule"

Garth Nicholson, Robert Ouvrier
Editorial

GDAP1 mutations in CMT4: axonal and demyelinating phenotypes?: The exception "proves the rule"

Garth Nicholson et al. Neurology. .
No abstract available

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Comment on

  • Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy.
    Nelis E, Erdem S, Van Den Bergh PY, Belpaire-Dethiou MC, Ceuterick C, Van Gerwen V, Cuesta A, Pedrola L, Palau F, Gabreëls-Festen AA, Verellen C, Tan E, Demirci M, Van Broeckhoven C, De Jonghe P, Topaloglu H, Timmerman V. Nelis E, et al. Neurology. 2002 Dec 24;59(12):1865-72. doi: 10.1212/01.wnl.0000036272.36047.54. Neurology. 2002. PMID: 12499475

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