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Identification of an alternative triglyceride biosynthesis pathwayGian‐Luca McLelland, Thijn R. Brummelkamp|Nature|2023Cited by 77
B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycanopathiesReza Maroofian, Hans van Bokhoven, Moniek Riemersma et al.|Genome Medicine|2017Cited by 14