The Syndrome of Inherited Partial SBP2 Deficiency in Humans-Reference-Cited by-同舟云学术

The Syndrome of Inherited Partial SBP2 Deficiency in Humans

Published:2010-04 Issue:7 Volume:12 Page:905-920
ISSN:1523-0864
Container-title:Antioxidants & Redox Signaling
language:en
Short-container-title:Antioxidants & Redox Signaling

Author:

Dumitrescu Alexandra M.¹,Cosmo Caterina Di¹,Liao Xiao-Hui¹,Weiss Roy E.¹²³,Refetoff Samuel¹²³⁴

Affiliation:

1. Department of Medicine, University of Chicago, Chicago, Illinois.

2. Department of Pediatrics and Committees on, University of Chicago, Chicago, Illinois.

3. Department of Molecular Medicine, University of Chicago, Chicago, Illinois.

4. Department of Genetics, University of Chicago, Chicago, Illinois.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Physiology,Biochemistry,Cell Biology,Clinical Biochemistry,Molecular Biology,Physiology,Biochemistry

Link

http://www.liebertpub.com/doi/pdf/10.1089/ars.2009.2892

Reference99 articles.

1. Regulation and function of selenoproteins in human disease

2. Physiological and genetic analyses of inbred mouse strains with a type I iodothyronine 5' deiodinase deficiency.

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