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- Erratum in:
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Nat Genet. 1997 Sep;17(1):122.
Congenital hypothyroidism caused by a mutation in the Na+/I- symporter.
PMID: 9171822 [PubMed - indexed for MEDLINE]
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Cited by 4 PubMed Central articles
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Molecular characterization of V59E NIS, a Na+/I- symporter mutant that causes congenital I- transport defect.
Reed-Tsur MD, De la Vieja A, Ginter CS, Carrasco N.
Endocrinology. 2008 Jun; 149(6):3077-84. Epub 2008 Mar 13.
[Endocrinology. 2008]
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ReviewGenetics of congenital hypothyroidism.
Park SM, Chatterjee VK.
J Med Genet. 2005 May; 42(5):379-89.
[J Med Genet. 2005]
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Mapping a dominant form of multinodular goiter to chromosome Xp22.
Capon F, Tacconelli A, Giardina E, Sciacchitano S, Bruno R, Tassi V, Trischitta V, Filetti S, Dallapiccola B, Novelli G.
Am J Hum Genet. 2000 Oct; 67(4):1004-7. Epub 2000 Sep 11.
[Am J Hum Genet. 2000]
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