Lataa...
A Novel De Novo Dominant Mutation in GJB2 Gene Associated with a Sporadic Case of Nonsyndromic Sensorineural Hearing Loss
Mutations in the GJB2 gene are the most common known cause of hereditary congenital hearing loss. Rapid genomic DNA extraction (RGDE) method was used for genomic DNA extraction. After amplification of coding region of CX26 gene with specific primers, expected PCR products with 724bp length were subj...
Tallennettuna:
| Julkaisussa: | Iran J Public Health |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Tehran University of Medical Sciences
2014
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4499094/ https://ncbi.nlm.nih.gov/pubmed/26171365 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|