diagnosis: congenital dyserythropoietic anemia type 2 due to compound heterozygote mutation in sec23b gene

Clicks: 183
ID: 254610
2015
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
Steady

Ranked #39 of 54 articles by views in proceedings of the international conference on iot in social, mobile, analytics and cloud, i-smac 2017

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
Abstract
Abstract is not available for this article.
Login to Search Abstract
Reference Key
demirciolu2015turkishdiagnosis: Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Fatih Demircioğlu;Mustafa Erkoçoğlu;Mustafa Dilek;Mervan Bekdaş;Sevil Göksügür;Semra Büyükkorkmaz;Seher Açar
Journal proceedings of the international conference on iot in social, mobile, analytics and cloud, i-smac 2017
Year 2015
DOI
10.4274/tjh.2014.0478
URL
Keywords

Citations

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

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