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Dive into the research topics of 'Rare missense mutations in P2RY11 in narcolepsy with cataplexy'. Together they form a unique fingerprint.- Sort by
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Matilda Degn, Yves Dauvilliers, Karin Dreisig, Régis Lopez, Corinne Pfister, Sylvain Pradervand, Birgitte Rahbek Kornum, Mehdi Tafti