Associated Papers
Variations in the Human Serum Albumin Gene: Molecular and Functional Aspects.
Caridi G et al.
International Journal of Molecular Sciences, 2022
35163085 (PubMed )
Supplement: ijms-23-01159-s001.zip › ijms-1498010-supplementary.pdf
A novel nonsense variation in the albumin gene (c.1309 A>T) causing analbuminaemia.
Caridi G et al.
British Journal of Biomedical Science, 2021
Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 cases.
Labrune P et al.
Human Genetics, 1994
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