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B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies.
scientific article published on 22 December 2017
Author/s
author: Lucas T Jae, Mahmood Reza Ashrafi, Yalda Jamshidi, Hans van Bokhoven, Marjolein H Willemsen, Tjitske Kleefstra, Arjan P M de Brouwer, Rolph Pfundt, Reza Maroofian
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Publication date
December 22, 2017
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