Mutation analysis and characterisation of F9 gene in haemophilia- B population of India-Reference-Cited by-同舟云学术

Mutation analysis and characterisation of F9 gene in haemophilia- B population of India

Published:2021-12-31 Issue:4 Volume:56 Page:252-258
ISSN:2287-979X
Container-title:BLOOD RESEARCH
language:en
Short-container-title:Blood Res

Author:

Kulkarni Sujayendra¹²,Hegde Rajat³,Hegde Smita³,Kulkarni Suyamindra S³,Hanagvadi Suresh⁴,Das Kusal K⁵,Kolagi Sanjeev⁶,Gai Pramod B³,Bulagouda Rudragouda¹

Affiliation:

1. Human Genetics Laboratory, Department of Anatomy, Shri B.M Patil Medical College, Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura, India

2. Division of Human Genetics (Central Research Lab), Bagalkot, India

3. Karnataka Institute for DNA Research (KIDNAR), Dharwad, India

4. Department of Pathology, J. J. M. Medical College, Davangere, Karnataka, India

5. Laboratory of Vascular Physiology and Medicine, Department of Physiology, Shri B. M. Patil Medical College, Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura, India

6. Department of Anatomy, S. Nijaliangappa Medical College, HSK Hospital and Research Center, Bagalkot, India

Publisher

The Korean Society of Hematology

Subject

Hematology

Link

https://pdf.medrang.co.kr/BR/2021/056/BR056-04-252.pdf

Reference29 articles.

1. Spectrum of F9 mutations in Chinese haemophilia B patients: identification of 20 novel mutations

2. Hemophilia treatment in historical perspective: a review of medical and social developments

3. Treatment of hemophilia: recombinant factors only? No

4. Hemophilia B: molecular pathogenesis and mutation analysis