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

Kulkarni S, Hegde R, Hegde S, Kulkarni SS, Hanagvadi S, Das KK, Kolagi S, Gai PB, Bulagouda R

Background Hemophilia B (HB) is an X-linked bleeding disorder resulting from coagulation factor IX defects. Over 3,000 pathogenic, HB-associated mutations in the F9 gene have been identified. We aimed to investigate...
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Genetic analysis of the postsynaptic transmembrane X-linked neuroligin 3 gene in autism

Hegde R, Hegde S, Kulkarni SS, Pandurangi A, Gai PB, Das KK

Autism is a complex neurodevelopmental disorder, the prevalence of which has increased drastically in India in recent years. Neuroligin is a type I transmembrane protein that plays a crucial role...
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