Identification of a structural requirement for thyroid Na+ /I− symporter (NIS) function from analysis of a mutation that causes human congenital hypothyroidism-Reference-Cited by-同舟云学术

Identification of a structural requirement for thyroid Na+ /I− symporter (NIS) function from analysis of a mutation that causes human congenital hypothyroidism

Published:1998-06-05 Issue:1 Volume:429 Page:36-40
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Levy Orlie,Ginter Christopher S,De la Vieja Antonio,Levy Daniel,Carrasco Nancy

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1016/S0014-5793(98)00522-5/fullpdf

Reference13 articles.

1. Congenital hypothyroidism caused by a mutation in the Na+/l− symporter

2. Cloning and characterization of the thyroid iodide transporter

3. Structure and function of the thyroid iodide transporter and its implications for thyroid disease

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