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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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| Publicado no: | Front Genet |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6478806/ https://ncbi.nlm.nih.gov/pubmed/31057599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00336 |
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