Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon

Clicks: 296
ID: 111138
2020
Free PDF
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #8 of 22 articles by views in clinical immunology (orlando, fla)

Most read Least read

Bar heights use a square-root scale.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Sign in to mint
Abstract
The patients are above the optimal age for transplant in WAS, and it is difficult to identify one or more donors for four patients, therefore, they represent ideal candidates for gene therapy or interleukin-2 therapy.
Reference Key
r2020clinicalwiskott-aldrich Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Mansour R;El-Orfali Y;Saber A;Noun D;Youssef N;Youssef Y;Hanna-Wakim R;Dbaibo G;Abboud M;Massaad MJ;;
Journal clinical immunology (orlando, fla)
Year 2020
DOI
DOI not found
URL
http://www.ncbi.nlm.nih.gov/pubmed/32814211
Keywords
National Center for Biotechnology Information NCBI NLM MEDLINE pubmed abstract nih national institutes of health national library of medicine pmid:32814211 doi:10.1016/j.clim.2020.108573 rana mansour youmna el-orfali michel j massaad

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

Comments

No comments yet. Be the first to comment on this article.