Associated Papers
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
Transmission of HIV-1 drug resistance mutations within partner-pairs: A cross-sectional study of a primary HIV infection cohort.
Stekler JD et al.
Plos Medicine, 2018
29584723 (PubMed )
Supplement: pmed.1002537.s002.doc
Select a paper to view details