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Browse result for Dejerine-Sottas syndrome
※ introduction Dejerine¨CSottas disease, also known as, Dejerine¨CSottas syndrome,[3] hereditary motor and sensory polyneuropathy type III, and Charcot¨CMarie¨CTooth disease type 3, is a hereditary neurological disorder characterized by damage to the peripheral nerves, demyelination, and resulting progressive muscle wasting and somatosensory loss. The condition is caused by mutations in various genes and currently has no known cure.[2]
Reference
Wiki: Dejerine-Sottas syndrome
Reference
Wiki: Dejerine-Sottas syndrome
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD04623 | P25189 | 4359 | MPZ | Myelin protein P0 | Homo sapiens |
| PTMD06108 | Q01453 | 5376 | PMP22 | Peripheral myelin protein 22 | Homo sapiens |
