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Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations
- Publication Year :
- 2015
-
Abstract
- Loss-of-function variants in ANKRD11 were identified as the cause of KBG syndrome, an autosomal dominant syndrome with specific dental, neurobehavioural, craniofacial and skeletal
Details
- Database :
- OAIster
- Notes :
- European Journal of Human Genetics vol. 23 no. 9, pp. 1176-1185, English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.ocn957101718
- Document Type :
- Electronic Resource
- Full Text :
- https://doi.org/10.1038.ejhg.2014.253