(Q28286095)

English

Mechanisms of inherited deficiencies of multiple UDP‐glucuronosyltransferase isoforms in two patients with Crigler‐Najjar syndrome, type I

scientific article published on July 1, 1992

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scholarly article

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Mechanisms of inherited deficiencies of multiple UDP-glucuronosyltransferase isoforms in two patients with Crigler-Najjar syndrome, type I (English)

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Mechanisms of inherited deficiencies of multiple UDP‐glucuronosyltransferase isoforms in two patients with Crigler‐Najjar syndrome, type I (English)

1 reference

10.1096/FASEBJ.6.10.1634050

https://api.crossref.org/works/10.1096/FASEBJ.6.10.1634050

18 October 2022

Crigler-Najjar syndrome

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based on heuristic

inferred from title

1 reference

10.1096/FASEBJ.6.10.1634050

https://api.crossref.org/works/10.1096/FASEBJ.6.10.1634050

18 October 2022

1 reference

10.1096/FASEBJ.6.10.1634050

https://api.crossref.org/works/10.1096/FASEBJ.6.10.1634050

18 October 2022

1 reference

10.1096/FASEBJ.6.10.1634050

https://api.crossref.org/works/10.1096/FASEBJ.6.10.1634050

18 October 2022

author name string

P. J. Bosma

1

1 reference

Europe PubMed Central

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18 October 2022

J. R. Chowdhury

2

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18 October 2022

T. J. Huang

3

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Europe PubMed Central

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18 October 2022

P. Lahiri

4

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18 October 2022

R. P. Elferink

5

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18 October 2022

H. H. Van Es

6

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18 October 2022

M. Lederstein

7

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18 October 2022

P. F. Whitington

8

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18 October 2022

P. L. Jansen

9

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18 October 2022

N. R. Chowdhury

10

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18 October 2022

language of work or name

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publication date

July 1992

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full work available at URL

http://www.fasebj.org/cgi/content/abstract/6/10/2859

online access status

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18 October 2022

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fasebj.6.10.1634050

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10.1096/FASEBJ.6.10.1634050

https://api.crossref.org/works/10.1096/FASEBJ.6.10.1634050

18 October 2022

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6

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10

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2859-63

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