A carregar...
Three families with ‘de novo’ m.3243A > G mutation
The m.3243A > G mutation is the most prevalent, disease-causing mitochondrial DNA (mtDNA) mutation. In a national cohort study of 48 families harbouring the m.3243A > G mutation, we identified three families in which the mutation appeared to occur sporadically within these families. In this re...
Na minha lista:
| Publicado no: | BBA Clin |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4900294/ https://ncbi.nlm.nih.gov/pubmed/27331024 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbacli.2016.04.007 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|