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Article

UGT1A1 genotype in a white boy with Crigler-Najjar syndrome type 2.

Journal of pediatric gastroenterology and nutrition - 1 Nov 2012

Peña Luis, Pico Miguel, Rosatelli Cristina, Meloni Antonella, Del Río Elisabeth, Tizzano Eduardo F, Baiget Montserrat

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PMID: 22722682
DOI: 10.1097/MPG.0b013e318234ecd9

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UGT1A1 genotype in a white boy with Crigler-Najjar syndrome type 2.PMID 22722682Read ↗

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Identification of an A-to-G missense mutation in exon 2 of the UGT1 gene complex that causes Crigler-Najjar syndrome type 2.Semantic proximity Read ↗

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Identification of three novel variants in the UGT1A1 gene as a cause of Crigler-Najjar syndrome type 1Semantic proximity Read ↗

Update on a previously reported missense mutation: The c.1160 C>A mutation in the UGT1A1 gene result in Crigler-Najjar syndrome type 1.Semantic proximity Read ↗

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UGT1A1 gene mutation due to Crigler-Najjar syndrome in Iranian patients: identification of a novel mutation.Semantic proximity Read ↗

[Genetic analysis of a child affected with Crigler-Najjar syndrome type II].Semantic proximity Read ↗

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Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation.Semantic proximity Read ↗

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