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Inherited Neuropathies: From Gene to Disease
Inherited disorders of peripheral nerves represent a common group of neurologic diseases. Charcot‐Marie‐Tooth neuropathy type 1 (CMT1) is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17 (CMT1A), chromosome 1 (CMT1B) and to another unknow...
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| Gepubliceerd in: | Brain Pathol |
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| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Blackwell Publishing Ltd
2006
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8098306/ https://ncbi.nlm.nih.gov/pubmed/10219749 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1750-3639.1999.tb00230.x |
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