B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycanopathies
Reza Maroofian(National Hospital for Neurology and Neurosurgery), Hans van Bokhoven(Radboud University Nijmegen), Benno Küsters(Radboud University Nijmegen), Mojila Nasseri, Lucas T. Jae(Ludwig-Maximilians-Universität München), Thijn R. Brummelkamp(The Netherlands Cancer Institute), Arjan P.M. de Brouwer(Radboud University Nijmegen), Mahmoud Reza Ashrafi(Children's Medical Center), Mohammad Reza Abbaszadegan(Mashhad University of Medical Sciences), Narges Zhianabed, Moniek Riemersma(Radboud University Nijmegen), Marjolein H. Willemsen(Radboud University Nijmegen), Yalda Jamshidi(St George's, University of London), W.M. Wissink-Lindhout(Radboud University Nijmegen), Mohammad Yahya Vahidi Mehrjardi(Shahid Sadoughi University of Medical Sciences and Health Services), Tjitske Kleefstra(Netherlands Institute for Neuroscience), Michèl A.A.P. Willemsen(Radboud University Nijmegen), Dirk J. Lefeber(Radboud University Nijmegen), Rolph Pfundt(University Medical Center Groningen)
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