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A Rare Case Report of Crigler Najjar Syndrome Type II

Crigler-Najjar syndrome is an inborn error of metabolism caused by a point mutation in one of the five exons of UGT1A1 gene, the product of which is responsible for elimination of bilirubin via bile. A number of hyperbilirubinemia disorders similar to Crigler-Najjar syndrome are reported, but they d...

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Detalles Bibliográficos
Autores principales:	Abdul Raffay, Eusha, Liaqat, Ayesha, Khan, Maria, Awan, Ali I, Mand, Bakhat
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880822/ https://www.ncbi.nlm.nih.gov/pubmed/33604208 http://dx.doi.org/10.7759/cureus.12669

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