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Autor:
Nicholas J. Andersen, Surender Rajasekaran, Jeremy W. Prokop, Nick Lannen, Brad Betz, Renee Jordan, Steven T. DeRoos, Laurie H. Seaver
Publikováno v:
Pediatric Neurology. 89:26-30
Background Infantile epileptic encephalopathy is a heterogeneous condition that has been associated with variants in more than 200 genes. The variability in findings and prognosis creates challenges to making the correct diagnosis and initiating the