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Dive into the research topics of 'CDKL5 mutations as a cause of severe epilepsy in infancy: Clinical and electroencephalographic long-term course in 4 patients'. Together they form a unique fingerprint.- Sort by
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Johanna Jähn*, Almuth Caliebe, Sarah Von Spiczak, Rainer Boor, Irina Stefanova, Ulrich Stephani, Ingo Helbig, Hiltrud Muhle