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
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant.
Caridi G et al.
Annals of Clinical Biochemistry, 2016
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family.
Caridi G et al.
Biochemia Medica, 2016
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