Associated Papers
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
Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A).
Dongerdiye R et al.
Journal of Clinical Pathology, 2019
PhenoHM: human-mouse comparative phenome-genome server.
Sardana D et al.
Nucleic Acids Research, 2010
20507906 (PubMed )
Supplement: gkq472_nar-00429-web-b-2010-File006.xls › MPO_to_OMIM_allelic_Variants
[Rare case of hereditary nonspherocytic anemia caused by glyceraldehydephosphate dehydrogenase deficiency in erythrocytes].
Reznik BIa et al.
Problemy Gematologii I Perelivaniia Krovi, 1972
A new variant of adenylate kinase (delG138) associated with severe hemolytic anemia.
Fermo E et al.
Blood Cells, Molecules & Diseases, 0
Select a paper to view details