Associated Papers
Variations in the Human Serum Albumin Gene: Molecular and Functional Aspects.
Caridi G et al.
International Journal of Molecular Sciences, 2022
Recurrent Hypoglycemia in a Case of Congenital Analbuminemia.
Litzel M et al.
Case Reports in Endocrinology, 2020
Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.
Minchiotti L et al.
Frontiers in Genetics, 2019
Human serum albumin isoforms: genetic and molecular aspects and functional consequences.
Kragh-Hansen U et al.
Biochimica Et Biophysica Acta, 2013
Congenital analbuminaemia: molecular defects and biochemical and clinical aspects.
Minchiotti L et al.
Biochimica Et Biophysica Acta, 2013
Mutations and polymorphisms of the gene of the major human blood protein, serum albumin.
Minchiotti L et al.
Human Mutation, 2008
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