Severe Congenital Factor X Deficiency in an Indian Child With a Concomitant Novel <i>ITGA2</i> Variant

The authors declare no conflicts of interest. Supporting data is available with the corresponding author and will be made available upon reasonable request

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Publication Details

Journal
Haemophilia
Published
2026-03-12
DOI
https://doi.org/10.1111/hae.70262
Primary Topic
Hemophilia Treatment and Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Severe Congenital Factor X Deficiency in an Indian Child With a Concomitant Novel ITGA2 Variant

Debadrita Ray, Chander Hans, Jasmina Ahluwalia, Rinki Das et al.
Haemophilia
Hemophilia Treatment and Research
article

Severe Congenital Factor X Deficiency in an Indian Child With a Concomitant Novel ITGA2 Variant

Debadrita Ray, Chander Hans, Jasmina Ahluwalia, Rinki Das, Narender Kumar, Manu Jamwal, Vasant Kumar, Vanita Jain
article en

Abstract

The authors declare no conflicts of interest. Supporting data is available with the corresponding author and will be made available upon reasonable request

Haemophilia
Post Graduate Institute of Medical Education and Research (IN)
Gender equality
Openalex Percentile: Top 24%
Hemophilia Treatment and Research
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