Literature DB >> 75612

[Treatment of Crigler-Najjar's congenital familial non-hemolytic jaundice with kernicterus].

E Plöchl, W Hohenwallner.   

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Year:  1978        PMID： 75612

Source DB:  PubMed          Journal:  Wien Med Wochenschr        ISSN： 0043-5341


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1.  UGT1A1 gene mutation due to Crigler-Najjar syndrome in Iranian patients: identification of a novel mutation.

Authors:  Javad Mohammadi Asl; Mohammad Amin Tabatabaiefar; Hamid Galehdari; Kourosh Riahi; Mohammad Hosein Masbi; Zohre Zargar Shoshtari; Fakher Rahim
Journal:  Biomed Res Int       Date:  2013-10-28       Impact factor: 3.411
  1 in total

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