Inviting an author to review:
Find an author and click ‘Invite to review selected article’ near their name.
Search for authorsSearch for similar articles
12
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Tetratricopeptide repeat domain 7A (TTC7A) mutation in a newborn with multiple intestinal atresia and combined immunodeficiency.

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          In the past year, two centers reported autosomal recessive mutations in tetratricopeptide repeat domain 7A (TTC7A) gene in patients with multiple intestinal atresia and immunodeficiency. Here, we present clinical progress of an infant with multiple intestinal atresia and combined immunodeficiency who carries novel compound heterozygote mutations in TTC7A gene.

          Related collections

          Author and article information

          Journal
          J. Clin. Immunol.
          Journal of clinical immunology
          1573-2592
          0271-9142
          Aug 2014
          : 34
          : 6
          Affiliations
          [1 ] Division of Allergy and Immunology, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
          Article
          10.1007/s10875-014-0067-7
          24931897
          031d5bf1-6dbc-42e6-89cb-cc86896b710e
          History

          Comments

          Comment on this article