TTC7A: Steward of Intestinal Health
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
Reference73 articles.
1. Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia;Samuels;J Med Genet,2013
2. Whole exome sequencing identifies TTC7A mutations for combined immunodeficiency with intestinal atresias;Chen;J Allergy Clin Immunol,2013
3. Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease;Avitzur;Gastroenterology,2014
4. Tetratricopeptide repeat domain 7A (TTC7A) mutation in a newborn with multiple intestinal atresia and combined immunodeficiency;Agarwal;J Clin Immunol,2014
5. TTC7A mutations disrupt intestinal epithelial apicobasal polarity;Bigorgne;J Clin Invest,2014
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