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- '''Peripheral nerve myelin protein 22 (PMP22)''' is clinically significant in several genetic [[peripheral neurop3 KB (430 words) - 11:58, 12 June 2010
- 342 bytes (44 words) - 14:23, 31 January 2010
- 294 bytes (33 words) - 11:40, 18 February 2010
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- ...by loss of myelin. Genetic diseases involving a defect of the coding for [[peripheral nerve myelin protein 22]], such as [[Charcot-Marie-Tooth disease]], also display abnormal myelin.772 bytes (112 words) - 17:09, 21 March 2024
- {{r|Peripheral nerve myelin protein 22}}472 bytes (55 words) - 19:10, 2 October 2013
- The genetic abnormalities is associated with the coding for [[peripheral nerve myelin protein 22]]; additional subtypes have been discovered. It is most an autosomal domina801 bytes (118 words) - 13:31, 12 June 2010
- '''Peripheral nerve myelin protein 22 (PMP22)''' is clinically significant in several genetic [[peripheral neurop3 KB (430 words) - 11:58, 12 June 2010