To advance the understanding of KCNQ2 encephalopathy genotype-phenotype relationships and to begin to assess the potential of selective KCNQ channel openers as targeted treatments.
KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients / Millichap, J.J., Park, K.L., Tsuchida, T., Ben Zeev, B., Carmant, L., Flamini, R., Joshi, N., Levisohn, P.M., Marsh, E., Nangia, S., Narayanan, V., Ortiz Gonzalez, X.R., Patterson, M.C., Pearl, P.L., Porter, B., Ramsey, K., Mcginnis, E.L., Taglialatela, M., Tracy, M., Tran, B., et al.. - In: NEUROLOGY. GENETICS. - ISSN 2376-7839. - 2:5(2016), p. e96. [10.1212/NXG.0000000000000096]
KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients
TAGLIALATELA, MAURIZIO;
2016
Abstract
To advance the understanding of KCNQ2 encephalopathy genotype-phenotype relationships and to begin to assess the potential of selective KCNQ channel openers as targeted treatments.| File | Dimensione | Formato | |
|---|---|---|---|
|
Neurol Genet-2016-Millichap-.pdf
solo utenti autorizzati
Tipologia:
Documento in Post-print
Licenza:
Accesso privato/ristretto
Dimensione
574.21 kB
Formato
Adobe PDF
|
574.21 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
