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A novel cause for primordial dwarfism revealed: defective tRNA modification
A mutation in the WDR4 gene, coding for a tRNA-modifying enzyme, leads to reduced levels of guanosine methylation in tRNA in patients with primordial dwarfism. See related Research article: http://www.genomebiology.com/2015/16/1/210.
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4591068/ https://www.ncbi.nlm.nih.gov/pubmed/26429597 http://dx.doi.org/10.1186/s13059-015-0786-y |