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, John J; Park, Kristen L; Tsuchida, Tammy; Ben Zeev, Bruria; Carmant, Lionel; Flamini, Robert; Joshi, Nishtha; Levisohn, Paul M; Marsh, Eric; Nangia, Srishti; Narayanan, Vinodh; Ortiz Gonzalez, Xilma R; Patterson, Marc C; Pearl, Phillip L; Porter, Brenda; Ramsey, Keri; Mcginnis, Emily L; Taglialatela, Maurizio; Tracy, Molly; Tran, Baouyen; Venkatesan, Charu; Weckhuysen, Sarah; Cooper, Edward C.. - 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 | |
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