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

Internet

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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