Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect-Reference-Cited by-同舟云学术

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Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect

Published:2022-12-26 Issue:2 Volume:29 Page:591-599
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Sharma Ritika¹,Jamwal Manu¹,Senee Hari Kishan¹,Singh Namrata¹^ORCID,Kumar Narender¹,Hans Chander¹,Kler Anita¹,Bansal Deepak²,Trehan Amita²,Malhotra Pankaj³,Ahluwalia Jasmina¹,Das Reena¹^ORCID

Affiliation:

1. Department of Hematology Postgraduate Institute of Medical Education and Research Chandigarh India

2. Department of Pediatrics (Hematology‐Oncology Unit) Postgraduate Institute of Medical Education and Research Chandigarh India

3. Department of Clinical Hematology and Medical Oncology Postgraduate Institute of Medical Education and Research Chandigarh India

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.14730

Reference34 articles.

1. Biochemical, molecular and clinical aspects of coagulation factor VII and its role in hemostasis and thrombosis

2. F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency

3. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders

4. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

5. Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India

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