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Dive into the research topics of 'Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects'. Together they form a unique fingerprint.- Sort by
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Carla Marini, Katia Hardies, Katia Hardies, Tiziana Pisano, Patrick May, Patrick May, Sarah Weckhuysen, Sarah Weckhuysen, Elena Cellini, Arvid Suls, Arvid Suls, Davide Mei, Rudi Balling, Peter D. Jonghe, Peter D. Jonghe, Peter D. Jonghe, Ingo Helbig, Ingo Helbig, Domenico Garozzo, Renzo Guerrini
Research output: Contribution to journal › Article › Academic › peer-review