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Dive into the research topics of 'Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease'. Together they form a unique fingerprint.- Sort by
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Gaetan Lesca, Nadia Boutry-Kryza, Bertrand de Toffol, Mathieu Milh, Dominique Steschenko, Martine Lemesle-Martin, Louis Maillard, Giovanni Foletti, Gabrielle Rudolf, Jørgen Erik Nielsen, Bjarke á Rogvi-Hansen, Jesper Erdal, Josette Mancini, Christel Thauvin-Robinet, Amel M'Rrabet, Dorothée Ville, Pierre Szepetowski, Emmanuel Raffo, Edouard Hirsch, Philippe Ryvlin