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2. Molecular basis of hereditary factor V deficiency in India: identification of four novel mutations and their genotype-phenotype correlation.

Author

Chapla A, Jayandharan GR, Sumitha E, Sankari Devi G, Shenbagapriya P, Nair SC, Viswabandya A, George B, Mathews V, and Srivastava A

Subjects
Child, Preschool, Consanguinity, DNA Mutational Analysis, Disease Progression, Factor V genetics, Factor V immunology, Factor V Deficiency epidemiology, Factor V Deficiency physiopathology, Female, Gene Frequency, Genetic Association Studies, Genetic Testing, Hemorrhage, Humans, India, Infant, Male, Mutation genetics, Prognosis, Factor V metabolism, Factor V Deficiency diagnosis, Factor V Deficiency genetics, Population Groups
Published
2011
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