Items where Author is "Raymond, F. Lucy"

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Journal Article

Zagaglia, Sara and Steel, Dora and Krithika, S. and Hernandez-Hernandez, Laura and Custodio, Helena M. and Gorman, Kathleen M. and Vezyroglou, Aikaterini and Møller, Rikke S. and King, Mary D. and Hammer, Trine B. and Spaull, Robert and Fazeli, Walid and Bartolomaeus, Tobias and Doummar, Diane and Keren, Boris and Mignot, Cyril and Bednarek, Nathalie and Cross, J. Helen and Mallick, Andrew A. and Sanchis-Juan, Alba and Basu, Anna and Raymond, F. Lucy and Lynch, Bryan J. and Majumdar, Anirban and Stamberger, Hannah and Weckhuysen, Sarah and Sisodiya, Sanjay M. and Kurian, Manju A. (2021) RHOBTB2 mutations expand the phenotypic spectrum of alternating hemiplegia of childhood. Neurology. ISSN 1526-632X

Steward, Charles A. and Roovers, Jolien and Suner, Marie-Marthe and Gonzalez, Jose M. and Uszczynska-Ratajczak, Barbara and Pervouchine, Dmitri and Fitzgerald, Stephen and Viola, Margarida and Stamberger, Hannah and Hamdan, Fadi F. and Ceulemans, Berten and Leroy, Patricia and Nava, Caroline and Lepine, Anne and Tapanari, Electra and Keiller, Don and Abbs, Stephen and Sanchis-Juan, Alba and Grozeva, Detelina and Rogers, Anthony S. and Diekhans, Mark and Guigó, Roderic and Petryszak, Robert and Minassian, Berge A. and Cavalleri, Gianpiero and Vitsios, Dimitrios and Petrovski, Slavé and Harrow, Jennifer and Flicek, Paul and Raymond, F. Lucy and Lench, Nicholas J. and De Jonghe, Peter and Mudge, Jonathan M. and Weckhuysen, Sarah and Sisodiya, Sanjay M. and Frankish, Adam (2019) Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A. npj Genomic Medicine, 4 (1). p. 31. ISSN 2056-7944

This list was generated on Mon Nov 29 02:17:27 2021 GMT.