HuGE Literature Finder
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DYRK1A mutations in two unrelated patients. European journal of medical genetics 2015 Mar 58 (3): 168-74. Ruaud Lyse, Mignot Cyril, Guët Agnès, Ohl Christelle, Nava Caroline, Héron Delphine, Keren Boris, Depienne Christel, Benoit Valérie, Maystadt Isabelle, Lederer Damien, Amsallem Daniel, Piard Juliet |
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. Molecular psychiatry 2015 Feb . van Bon B W M, Coe B P, Bernier R, Green C, Gerdts J, Witherspoon K, Kleefstra T, Willemsen M H, Kumar R, Bosco P, Fichera M, Li D, Amaral D, Cristofoli F, Peeters H, Haan E, Romano C, Mefford H C, Scheffer I, Gecz J, de Vries B B A, Eichler E |
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