Associated Papers
Human genetic disorders of sphingolipid biosynthesis.
Astudillo L et al.
Journal of Inherited Metabolic Disease, 2015
Functional characterisation of a complex mutation in the α(1,4)galactosyltransferase gene in Taiwanese individuals with p phenotype.
Wang YC et al.
Transfusion Medicine (oxford, England), 2011
Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection.
Hellberg A et al.
British Journal of Haematology, 2004
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