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Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia

Congenital analbuminemia (CAA) is an inherited, autosomal recessive disorder with an incidence of 1:1,000,000 live birth. Affected individuals have a strongly decreased concentration, or complete absence, of serum albumin. The trait is usually detected by serum protein electrophoresis and immunochem...

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Detalles Bibliográficos
Autores principales:	Minchiotti, Lorenzo, Caridi, Gianluca, Campagnoli, Monica, Lugani, Francesca, Galliano, Monica, Kragh-Hansen, Ulrich
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2019
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478806/ https://www.ncbi.nlm.nih.gov/pubmed/31057599 http://dx.doi.org/10.3389/fgene.2019.00336

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