Literature DB >> 10702824

A Caucasian boy with Gilbert's syndrome heterozygous for the (TA)(8) allele.

A Tsezou, M Tzetis, S Kitsiou, E Kavazarakis, A Galla, E Kanavakis.   

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Year:  2000        PMID： 10702824

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


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  2 in total

1.  UGT1A1*28 relationship with abnormal total bilirubin levels in chronic hepatitis C patients: Outcomes from a case-control study.

Authors:  Marcelo Moreira Tavares de Souza; Victor Van Vaisberg; Rodrigo Martins Abreu; Aline Siqueira Ferreira; Camila daSilvaFerreira; Paulo Dominguez Nasser; Helena Scavone Paschoale; Flair José Carrilho; Suzane Kioko Ono
Journal:  Medicine (Baltimore)       Date:  2017-03       Impact factor: 1.889

2.  Novel combined UGT1A1 mutations in Crigler Najjar Syndrome type I.

Authors:  Nawel Abdellaoui; Balkiss Abdelmoula; Rania Abdelhedi; Najla Kharrat; Mouna Tabebi; Ahmed Rebai; Nouha Bouayed Abdelmoula
Journal:  J Clin Lab Anal       Date:  2022-05-09       Impact factor: 3.124
  2 in total

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