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American Medical Association, JAMA Neurology, 3(76), p. 342

DOI: 10.1001/jamaneurol.2018.2941

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Identification of a Loss-of-Function Mutation in the Context of Glutaminase Deficiency and Neonatal Epileptic Encephalopathy

Journal article published in 2019 by Lynne Rumping, Benjamin Büttner, Oliver Maier, Holger Rehmann, Maarten Lequin, Jan-Ulrich Schlump, Bernhard Schmitt, Birgit Schiebergen-Bronkhorst, Hubertus C. M. T. Prinsen, Michele Losa, Ralph Fingerhut, Johannes R. Lemke, Fried J. T. Zwartkruis ORCID, Roderick H. J. Houwen, Judith J. M. Jans ORCID and other authors.
Distributing this paper is prohibited by the publisher
Distributing this paper is prohibited by the publisher

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