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
Congenital analbuminaemia: molecular defects and biochemical and clinical aspects.
Minchiotti L et al.
Biochimica Et Biophysica Acta, 2013
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia.
Caridi G et al.
European Journal of Clinical Investigation, 2013
A novel two bases deletion in the albumin gene causes analbuminaemia in a young Turkish man.
Caridi G et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2012
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