Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine development.

@article{Baechner1995WidespreadEO,
  title={Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine development.},
  author={D Baechner and Thomas Liehr and H. Hameister and H Altenberger and Holger Grehl and Ueli Suter and Bernd W. Rautenstrau\ss},
  journal={Journal of neuroscience research},
  year={1995},
  volume={42 6},
  pages={733-41}
}
The gene encoding the peripheral myelin protein PMP22 is affected by various mutations in the hereditary peripheral neuropathies Charcot-Marie-Tooth disease type 1A (CMT1A), Déjérine-Sottas syndrome (DSS) and hereditary neuropathy with liability to pressure palsies (HNPP). In contrast to the recent remarkable progress in the genetics of the PMP22 gene, the biological function of PMP22 remains largely unknown. In this report, we have confirmed by using in situ hybridization techniques that high… CONTINUE READING

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