Vinod Gupta

Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia

Vinod Gupta, Anuja Kulkarni, Prashant Warang et al. · Human Mutation · 2020 · 23 citations

Genetics, Pathology, Molecular Biology +16

Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients

Prabhakar Kedar, Vinod Gupta, Rashmi Dongerdiye et al. · Journal of Clinical Pathology · 2018 · 20 citations

Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction

Prabhakar Kedar, Rashmi Dongerdiye, Pooja Chilwirwar et al. · The Indian Journal of Pediatrics · 2019 · 20 citations

Genetic Disorder, Genetics, Inherited Metabolic Disease +9

Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I

Prabhakar Kedar, Vinod Gupta, Prashant Warang et al. · Hematology · 2018 · 18 citations · Full text

G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India

Rati Devendra, Vinod Gupta, Somashekhar S. Biradar et al. · Annals of Human Biology · 2019 · 10 citations · Full text