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Fatigue in patients with hereditary neuropathy with liability to pressure palsies
OBJECTIVE: Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) is caused by a heterozygous deletion of peripheral myelin protein‐22 (PMP22) gene resulting in focal sensorimotor deficits. Our lab has identified a disruption of myelin junctions in excessively permeable myelin that impairs...
Tallennettuna:
| Julkaisussa: | Ann Clin Transl Neurol |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7448142/ https://ncbi.nlm.nih.gov/pubmed/32856791 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51133 |
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