Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
2012
This journal suppl. is Special Issue: Abstracts of the 12th International Child Neurology Congress and the 11th Asian and Oceanian Congress of Child Neurology ... 2012
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
0
References
0
Citations
NaN
KQI