Rati Devendra
3PUBLICATIONS
7CO-AUTHORS
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Publications (3)
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|Mar 09, 2023
Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population.Rashmi Dongerdiye, Meghana Bokde, Tejashree Anil More
|Jan 04, 2023
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum.Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye
|Dec 14, 2019
G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India.Rati Devendra, Vinod Gupta, Somashekhar S Biradar
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