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