Lanean...
Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteins
The homoplasmic mitochondrial A1555G mutation in the 12S rRNA gene leads to a mitochondrial translation disorder associated with deafness. The absence of disease in non-cochlear tissues in all patients, and in the cochlea in some patients, is not well understood. We used a system-based approach, inc...
Gorde:
| Egile Nagusiak: | , , |
|---|---|
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2009
|
| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2728627/ https://ncbi.nlm.nih.gov/pubmed/19482502 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2009.05.003 |
| Etiketak: |
Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|