Literature DB >> 4775130

Dubin-Johnson Syndrome. Abnormal excretion of the isomers of urinary coproporphyrin by clinically unaffected family members.

J Ben-Ezzer, J Blonder, M Shani, U Seligsohn, C A Post, A Adam, A Szeinberg.   

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Year:  1973        PMID： 4775130

Source DB:  PubMed          Journal:  Isr J Med Sci        ISSN： 0021-2180


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  2 in total

1.  Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2.

Authors:  Lenka Slachtova; Ondrej Seda; Jana Behunova; Martin Mistrik; Pavel Martasek
Journal:  Eur J Hum Genet       Date:  2015-09-09       Impact factor: 4.246

2.  Dubin-Johnson syndrome in a neonate.

Authors:  F Nakata; K Oyanagi; M Fujiwara; H Sogawa; R Minami; K Horino; T Nakao; T Kondo
Journal:  Eur J Pediatr       Date:  1979       Impact factor: 3.183
  2 in total

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