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Intrafamilial heterogeneity of clinical phenotype of PRRT2 mutations.
- Source :
- European Journal of Paediatric Neurology; Jun2017 Supplement 1, Vol. 21, pe217-e217, 1p
- Publication Year :
- 2017
Details
- Language :
- English
- ISSN :
- 10903798
- Volume :
- 21
- Database :
- Supplemental Index
- Journal :
- European Journal of Paediatric Neurology
- Publication Type :
- Academic Journal
- Accession number :
- 123530950
- Full Text :
- https://doi.org/10.1016/j.ejpn.2017.04.1125