Associated Papers
A case report of a rare p phenotype individual and a review of molecular biological analysis of p phenotype in the Chinese population.
Wei X et al.
Transfusion Medicine (oxford, England), 2025
Novel A4GALT Variants Cause Rare p Phenotype and Recurrent Pregnancy Loss in a Chinese Individual.
Li G et al.
American Journal of Medical Genetics. Part A, 2025
Human genetic disorders of sphingolipid biosynthesis.
Astudillo L et al.
Journal of Inherited Metabolic Disease, 2015
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