학술논문
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency
Document Type
Article
Author
Tan, C.; Hynes, K.; Pham, D.H.; Corbett, M.; Shoubridge, C.; Kumar, R.; Nguyen, L.S.; Haan, E.; Gecz, J.; Shard, C.; Thomas, P.Q.; Ranieri, E.; Douglas, E.; Leach, D.; Buchanan, G.; Mcmahon, J.; Berkovic, S.F.; Scheffer, I.E.; Sadleir, L.; Specchio, N.; Marini, C.; Guerrini, R.; Moller, R.S.; Depienne, C.
Source
In: Human Molecular Genetics . (Human Molecular Genetics, 9 April 2015, 24(18):5250-5259)
Subject
Language
English
ISSN
14602083
09646906
09646906