B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycanopathies

RT @GenomeMedicine: B3GALNT2 mutations, intellectual disability, and muscular dystrophy-dystroglycanopathies: insights from whole #exome se…

RT @GenomeMedicine: B3GALNT2 mutations, intellectual disability, and muscular dystrophy-dystroglycanopathies: insights from whole #exome se…

RT @GenomeMedicine: B3GALNT2 mutations, intellectual disability, and muscular dystrophy-dystroglycanopathies: insights from whole #exome se…

B3GALNT2 mutations, intellectual disability, and muscular dystrophy-dystroglycanopathies: insights from whole #exome sequencing #RareDiseaseDay https://t.co/N7h0EqYer0 https://t.co/RmpTVhRFrs