Forkhead box protein E1

[1]. Isabella Venza, et al. MSX1 and TGF-beta3 are novel target genes functionally regulated by FOXE1. Hum Mol Genet. 2011 Mar 1;20(5):1016-25. [Content Brief]

[2]. Aurore Carré, et al. A novel FOXE1 mutation (R73S) in Bamforth-Lazarus syndrome causing increased thyroidal gene expression. Thyroid. 2014 Apr;24(4):649-54. [Content Brief]

[3]. R J Clifton-Bligh, et al. Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia. Nat Genet. 1998 Aug;19(4):399-401. [Content Brief]

[4]. Joana S Pereira, et al. Identification of a novel germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC). Endocrine. 2015 May;49(1):204-14. [Content Brief]

[5]. I Baris, et al. A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis. J Clin Endocrinol Metab. 2006 Oct;91(10):4183-7. [Content Brief]

[6]. Mireille Castanet, et al. A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate. Hum Mol Genet. 2002 Aug 15;11(17):2051-9. [Content Brief]

[7]. Mireille Castanet, et al. Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism. J Clin Endocrinol Metab. 2010 Aug;95(8):4031-6. [Content Brief]

[8]. In-Nee Kang, et al. Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis. Biochem Genet. 2010 Feb;48(1-2):141-51. [Content Brief]