Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene

Detalles Bibliográficos
Autores principales: Caridi, Gianluca, Maout, Abdelbasset, Artan, Reha, Campagnoli, Monica, Lugani, Francesca, Abada, Mohamed El Amine, Sayar, Ersin, Galliano, Monica, Minchiotti, Lorenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Laboratory Medicine 2018
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736683/
https://www.ncbi.nlm.nih.gov/pubmed/29214768
http://dx.doi.org/10.3343/alm.2018.38.2.185

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736683/
https://www.ncbi.nlm.nih.gov/pubmed/29214768
http://dx.doi.org/10.3343/alm.2018.38.2.185

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