학술논문
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene
Document Type
Article
Author
Panagiotakaki, E.; Arzimanoglou, A.; Tiziano, F.D.; Di Pietro, L.; Mikati, M.A.; Vijfhuizen, L.S.; Harder, A.V.E.; van den Maagdenberg, A.M.J.M.; Nicole, S.; Lesca, G.; Abiusi, E.; Novelli, A.; Walley, N.M.; De Grandis, E.; Poulat, A.-L.; Portes, V.D.; Lépine, A.; Nassogne, M.-C.; Vavassori, R.; Koenderink, J.; Thompson, C.H.; George, A.L.; Gurrieri, F.; Heinzen, E.L.
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, February 2024, 32(2):224-231)
Subject
Language
English
ISSN
14765438
10184813
10184813