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Congenital hypothyroidism caused by a mutation in the Na+/I- symporter.

Authors: Fujiwara, H  Tatsumi, K  Miki, K  Harada, T  Miyai, K  Takai, S  Amino, N 
Citation: Fujiwara H, etal., Nat Genet. 1997 Jun;16(2):124-5.
Pubmed: (View Article at PubMed) PMID:9171822
DOI: Full-text: DOI:10.1038/ng0697-124



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RGD Object Information
RGD ID: 1624273
Created: 2007-05-07
Species: All species
Last Modified: 2007-05-07
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.