Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1966733 | Clinica Chimica Acta | 2017 | 5 Pages |
Abstract
Gel-based mutation detection and DNA sequencing substantiate the clinical diagnosis of congenital analbuminemia in our patient and show that the condition is caused by a novel mutation within the ALB gene. These results contribute to shed light on the molecular basis of this rare condition.
Keywords
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Biochemistry
Authors
Monica Dagnino, Gianluca Caridi, Zeki Aydin, Savas Ozturk, Zeynep Karaali, Rumeyza Kazancioglu, Kivanc Cefle, Meltem Gursu, Monica Campagnoli, Monica Galliano, Lorenzo Minchiotti,