Cargando...
Mitochondrial DNA Mutation Screening in an Ethnically Diverse Nonsyndromic Deafness Cohort
Deafness is a heterogeneous trait with many known genetic and environmental causes. Hereditary hearing loss is an extremely common disorder in the general population. Mutations in mitochondrial DNA (mtDNA) are known to be associated with nonsyndromic deafness (NSD) and syndromic deafness. The object...
Gardado en:
| Main Authors: | , , , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Mary Ann Liebert, Inc.
2012
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3438807/ https://ncbi.nlm.nih.gov/pubmed/22853457 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2011.0365 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|