Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper IgE
<p>Highlights: Whole exome sequencing identified the underlying defect in a patient with combined immunodeficiency.</p><p>A novel compound heterozygous DOCK8 mutation was identified.</p><p>Expression of a truncated DOCK8 protein with hypomorphic function was identified....
Hlavní autoři: | Kienzler, A, van Schouwenburg, P, Taylor, J, Marwah, I, Sharma, R, Noakes, C, Thomson, K, Sadler, R, Segal, S, Ferry, B, Blair, E, Chapel, H, Patel, S |
---|---|
Médium: | Journal article |
Vydáno: |
Elsevier
2015
|
Podobné jednotky
-
Hyper IgE Syndrome
Autor: Poonam Marwah, a další
Vydáno: (2019-03-01) -
RARE PRIMARY IMMUNODEFICIENCY – HYPER-IgE-SYNDROME: CASE REPORT AND LITERATURE REVIEW
Autor: Nikolai Vasil'evich Sobotyuk, a další
Vydáno: (2013-01-01) -
The genetics of hyper IgE syndromes
Autor: Randa AlYafie, a další
Vydáno: (2025-02-01) -
Hyper-IgE syndrome. Lessons from function and defects of STAT-3 or DOCK-8
Autor: Julio César Alcántara-Montiel, a další
Vydáno: (2016-10-01) -
Giant Herpes Labialis in a Child with DOCK8-deficient Hyper-IgE Syndrome
Autor: Ayşe Metin, a další
Vydáno: (2016-02-01)