Associated Papers
Variations in the Human Serum Albumin Gene: Molecular and Functional Aspects.
Caridi G et al.
International Journal of Molecular Sciences, 2022
Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.
Minchiotti L et al.
Frontiers in Genetics, 2019
Congenital analbuminaemia: molecular defects and biochemical and clinical aspects.
Minchiotti L et al.
Biochimica Et Biophysica Acta, 2013
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient.
Dagnino M et al.
European Journal of Clinical Investigation, 2010
A novel nonsense mutation in the albumin gene (c.1275 C>A) causing analbuminemia in a Tunisian boy.
Caridi G et al.
Clinical Chemistry and Laboratory Medicine, 2009
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