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Proteomics plus genomics approaches in primary immunodeficiency: the case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome

โœ Scribed by D. Zennaro; E. Scala; D. Pomponi; E. Caprini; D. Arcelli; E. Gambineri; G. Russo; A. Mari


Book ID
108701503
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
377 KB
Volume
167
Category
Article
ISSN
0009-9104

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The immune dysregulation, polyendocrinop
โœ Ochs, Hans D.; Bennett, Craig L.; Christie, Jacinda; Ramsdell, Fred; Brunkow, Ma ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› Nature Publishing Group ๐ŸŒ English โš– 44 KB

The gene WAS, contained in this interval, was excluded as a candidate for IPEX (refs. 1,2). The scurfy syndrome in mice 3 shares phenotypic features with IPEX and maps to a region of conserved synteny on the mouse X chromosome. Human and mouse FOXP3 were recently identified by positional cloning and