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POLG1 Mutations and Charcot-Marie-Tooth Disease Cover

POLG1 Mutations and Charcot-Marie-Tooth Disease

Open Access
|Feb 2008

References

  1. Harrower T Stewart JD Hudson G Houlden H Warner G O’Donovan DG POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease Arch Neurol 2008 Jan 65 1 133 6 10.1001/archneurol.2007.4 18195151
  2. Braathen GJ Sand JC Bukholm G Russell MB Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease BMC Neurol 2007 Jul 9 7 19 28 17620124
Language: English
Page range: 13 - 13
Published on: Feb 1, 2008
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services

© 2008 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.