Associated Papers
Severe Hemolytic Anemia due to Erythrocyte Adenylate Kinase Deficiency due to a Novel Missense Mutation (c.518T>G).
Panda K et al.
Indian Journal of Pediatrics, 2024
Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population.
Dongerdiye R et al.
Annals of Hematology, 2023
Red cell adenylate kinase deficiency in China: molecular study of 2 new mutations (413G > A, 223dupA).
He S et al.
Bmc Medical Genomics, 2022
Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family.
Dongerdiye R et al.
Bmc Medical Genomics, 2021
[Rare case of hereditary nonspherocytic anemia caused by glyceraldehydephosphate dehydrogenase deficiency in erythrocytes].
Reznik BIa et al.
Problemy Gematologii I Perelivaniia Krovi, 1972
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