(Q24685524)

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Functional role of the 503F variant of the organic cation transporter OCTN1 in Crohn's disease

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Functional role of the 503F variant of the organic cation transporter OCTN1 in Crohn's disease (English)

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D Taubert

1

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G Grimberg

series ordinal

2

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N Jung

series ordinal

3

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A Rubbert

series ordinal

4

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E Schömig

series ordinal

5

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language of work or name

English

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publication date

October 2005

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published in

Gut

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volume

54

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issue

10

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page(s)

1505-6

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cites work

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7 April 2017

Functional variants of OCTN cation transporter genes are associated with Crohn disease

1 reference

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PubMed Central

reference URL

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An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

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Identifiers

DOI

10.1136/GUT.2005.076083

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PMC publication ID

1774715

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PubMed publication ID

16162962

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ResearchGate publication ID

7599981

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(Q24685524)

Functional role of the 503F variant of the organic cation transporter OCTN1 in Crohn's disease

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