Molecular pathology of haemophilia A in Indian patients: Identification of 11 novel mutations
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference34 articles.
1. Comprehensive care for haemophilia around the world;Evatt;Haemophilia,2004
2. Intron 22 inversions in factor VIII gene in Indian haemophiliacs;Shetty;Thromb Haemost,1998
3. http://www.europium.csc.mrc.ac.uk/WebPages/PublicFiles/MutationSummary.xls HAMSTeRS mutation database.
4. Major disorganization of factor VIII gene as a cause of severe haemophilia A in Indian patients;Shetty;Am J Hematol,2004
5. Carrier detection and prenatal diagnosis in haemophilia in India: Realities and challenges;Ghosh;Haemophilia,2002
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2. Spectrum of Causative Mutations in Patients with Hemophilia A in Russia;Genes;2023-01-19
3. F8 gene mutation profile in Indian hemophilia A patients: Identification of 23 novel mutations and factor VIII inhibitor risk association;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;2016-04
4. Abnormal coagulation factor VIII transcript in a Tennessee Walking Horse colt with hemophilia A;Veterinary Clinical Pathology;2016-01-14
5. Molecular analysis of Bombay phenotype cases seen in India;ISBT Science Series;2015-11
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