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Regulation of the neuropathy-associated Pmp22 gene by a distal super-enhancer
Peripheral nerve myelination is adversely affected in the most common form of the hereditary peripheral neuropathy called Charcot-Marie-Tooth Disease. This form, classified as CMT1A, is caused by a 1.4 Mb duplication on chromosome 17, which includes the abundantly expressed Schwann cell myelin gene,...
Gorde:
| Argitaratua izan da: | Hum Mol Genet |
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| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Oxford University Press
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6077802/ https://ncbi.nlm.nih.gov/pubmed/29771329 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy191 |
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