(Q24540140)

English

Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome

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scholarly article

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Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome (English)

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Dubin-Johnson syndrome

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based on heuristic

inferred from title

author name string

S Toh

1

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M Wada

2

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T Uchiumi

3

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A Inokuchi

4

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Y Makino

5

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Y Horie

6

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Y Adachi

7

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S Sakisaka

8

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M Kuwano

9

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language of work or name

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publication date

March 1999

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American Journal of Human Genetics

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64

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3

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739-46

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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

1 reference

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1 reference

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A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome

1 reference

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1 reference

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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