Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencing
| Image |  |
|---|---|
| Description | scientific article published on 08 August 2013 |
| Author/s |
author: Polona Le Quesne Stabej Linda M Luxon Mireille Claustres Maria Bitner-Glindzicz |
| Publication date | August 8, 2013 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |