Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family

por Dongerdiye, Rashmi, Sampagar, Abhilasha, Devendra, Rati, Warang, Prashant, Kedar, Prabhakar
Publicado 2021

A novel nine base deletion mutation in NADH-cytochrome b5 reductase gene in an Indian family with recessive congenital methemoglobinemia-type-II

por Warang, Prashant, Kedar, Prabhakar, Sivanandam, S., Jothilakshmi, K., Sumathi, R., Colah, Roshan
Publicado 2015