Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies
By George P. Patrinos, Belinda Giardine, C. Riemer, Webb Miller, D. Chui, N. Anagnou, H. Wajcman, Ross C. Hardison. Nucleic Acids Res., 2004
410 citations recorded by the source corpus.
Subfields: Genetics, Hematology
View Paper: https://www.semanticscholar.org/paper/9890e1c6e0720ce9e82a0ec64ea8325d34f86e76
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In Genetics
- Pauline Crystal Ng
- Steven Henikoff
- Prateek Kumar
- Yana Bromberg
- Burkhard Rost
- Mauno Vihinen
- David N. Cooper
- Agnes P. Chan
Citations in the corpus
- Predicting the effects of amino acid substitutions on protein function. (2006, background): “Popular nonneutral sets include data from laboratory mutagenesis experiments (36, 49, 54, 80), human disease proteins where many mutations have been characterized (3, 21, 22, 25, 32, 50, 55, 70), and human disease databases such as OMIM, HGMD, or SwissProt (1, 24, 62), which contain AASs that have b”