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EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus
- Source :
- European Journal of Human Genetics; 1325; 9; 1018-4813; 11; vol. 21; ~European Journal of Human Genetics~1325~9~~~1018-4813~11~21~~
- Publication Year :
- 2013
-
Abstract
- Contains fulltext : 125367.pdf (publisher's version ) (Open Access)
Details
- Database :
- OAIster
- Journal :
- European Journal of Human Genetics; 1325; 9; 1018-4813; 11; vol. 21; ~European Journal of Human Genetics~1325~9~~~1018-4813~11~21~~
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1284084707
- Document Type :
- Electronic Resource