Unusually mild tuberous sclerosis phenotype is associated with<i>TSC2</i>R905Q mutation
Anna Jansen(Vrije Universiteit Brussel), Eva Andermann(Montreal Neurological Institute and Hospital), Daniela D’Agostino(McGill University Health Centre), Elisabeth A. Thiele(Harvard University), Dicky Halley(Norwegian Institute for Nature Research), Mark Nellist(Erasmus MC), Denis Melanson(McGill University), Miriam Goedbloed(Erasmus University Rotterdam), Őzgür Sancak(Erasmus University Rotterdam), Mary McQueen(Harvard University), Donatella Tampieri(Queen's University), Mark Gans(McGill University), François Dubeau(Université de Sherbrooke), Massimo Pandolfo(McGill University), Robert K. Koenekoop(McGill University Health Centre), AmanPreet Badhwar(Montreal Neurological Institute and Hospital), David J. Kwiatkowski(Brigham and Women's Hospital), Ralph Wilkinson(McGill University), Ans M.W. van den Ouweland(Erasmus University Rotterdam), Frédérick Andermann(University Hospital of Lausanne), Penelope Roberts(Brigham and Women's Hospital), Gabriella Gobbi(McGill University), Anneke Maat‐Kievit(Erasmus University Rotterdam), Katherine B. Sims(Massachusetts General Hospital)
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