Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis-Reference-Cited by-同舟云学术

Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis

Published:2007-08-24 Issue:5 Volume:122 Page:467-476
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Carré Aurore,Castanet Mireille,Sura-Trueba Sylvia,Szinnai Gabor,Van Vliet Guy,Trochet Delphine,Amiel Jeanne,Léger Juliane,Czernichow Paul,Scotet Virginie,Polak Michel

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-007-0420-5.pdf

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4. Amiel J, Laudier B, Attie-Bitach T, Trang H, de Pontual L, Gener B, Trochet D, Etchevers H, Ray P, Simonneau M, Vekemans M, Munnich A, Gaultier C, Lyonnet S (2003) Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet 33:459–461

5. Baris I, Arisoy AE, Smith A, Agostini M, Mitchell CS, Park SM, Halefoglu AM, Zengin E, Chatterjee VK, Battaloglu E (2006) A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis. J Clin Endocrinol Metab 91(10):4183–4187

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