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

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

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article científic

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bilimsel makale

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scientific article published on 09 September 2015

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Genetic and biochemical study ...... er effect of deletion in ABCC2

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Genetic and biochemical study ...... r effect of deletion in ABCC2.

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Genetic and biochemical study ...... er effect of deletion in ABCC2

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Genetic and biochemical study ...... r effect of deletion in ABCC2.

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Genetic and biochemical study ...... er effect of deletion in ABCC2

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Genetic and biochemical study ...... r effect of deletion in ABCC2.

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P1476

Genetic and biochemical study ...... er effect of deletion in ABCC2

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P2093

Jana Behunova

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Lenka Slachtova

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Martin Mistrik

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Mutations in the canilicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome

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P2888

ejhg.2015.181

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704-709

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P31

scholarly article

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10.1038/EJHG.2015.181

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P478

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Pavel Martasek

Ondřej Šeda

P577

2015-09-09T00:00:00Z

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P698

26350512

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P932

4930088

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