Literature DB >> 18056007

Evaluation of genetic markers linked to hemophilia A locus: an Indian experience.

Atreyee Saha1, Saibal Mukherjee, Mahua Maulik, Giriraj Ratan Chandak, Kunal Ray.   

Abstract

Hemophilia A is an X-linked recessive bleeding disorder caused by defects in factor VIII gene (F8). Our study examines variations of single nucleotide polymorphism (SNP) in F8 in the Indian population and establishes the utility of a combination of SNP and microsatellite markers for the successful identification of carriers in the affected families.

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Year:  2007        PMID: 18056007     DOI: 10.3324/haematol.11545

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  3 in total

1.  IGVBrowser--a genomic variation resource from diverse Indian populations.

Authors:  Ankita Narang; Rishi Das Roy; Amit Chaurasia; Arijit Mukhopadhyay; Mitali Mukerji; Debasis Dash
Journal:  Database (Oxford)       Date:  2010-09-15       Impact factor: 3.451

2.  Treatment of an intraoral bleeding in hemophilic patient with a thermoplastic palatal stent - A novel approach.

Authors:  Nidhi Madan; Arun Rathnam; Neeti Bajaj
Journal:  Int J Crit Illn Inj Sci       Date:  2011-01

Review 3.  Epidemiology & social costs of haemophilia in India.

Authors:  Anita Kar; Supriya Phadnis; Sumedha Dharmarajan; Juhi Nakade
Journal:  Indian J Med Res       Date:  2014-07       Impact factor: 2.375

  3 in total

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