Widespread expression of the peripheral myelin protein‐22 gene (<i>pmp</i>22) in neural and non‐neural tissues during murine development

Abstract excerpt

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...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Botulinum Toxin and Related Neurological Disorders
• Share to Hereditary Neurological Disorders
• Share to Neurological diseases and metabolism