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The topology, structure and PE interaction of LITAF underpin a Charcot-Marie-Tooth disease type 1C
BACKGROUND: Mutations in Lipopolysaccharide-induced tumour necrosis factor-α factor (LITAF) cause the autosomal dominant inherited peripheral neuropathy, Charcot-Marie-Tooth disease type 1C (CMT1C). LITAF encodes a 17 kDa protein containing an N-terminal proline-rich region followed by an evolutiona...
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| Publicado no: | BMC Biol |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5142333/ https://ncbi.nlm.nih.gov/pubmed/27927196 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12915-016-0332-8 |
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