- Mutation analysis and characterisation of F9 gene in haemophilia- B population of India
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Kulkarni S, Hegde R, Hegde S, Kulkarni SS, Hanagvadi S, Das KK, Kolagi S, Gai PB, Bulagouda R
- KMID: 2524077
- Blood Res.
- 2021 Dec;56(4):252-258.
- doi: 10.5045/br.2021.2021016
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
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Hegde R, Hegde S, Kulkarni SS, Pandurangi A, Gai PB, Das KK
- KMID: 2524335
- Genomics Inform.
- 2021 Dec;19(4):e44.
- doi: 10.5808/gi.21029
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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