Article
Amino acids exchange obtained from CKD patients via Exome Sequencing differ radically from those of natural variants 1000 genome and genomAD databases
2024-04-30
Abstract excerpt
<title>Abstract</title> <p><italic><bold>Background:</bold></italic> Nonsynonymous mutations in the coding regions of human genes are responsible for phenotypic differences between humans and for their susceptibility to genetic disease. <italic><bold>Methods:</bold></italic><bold> </bold>We performed Exome sequencing on CKD patients’ genomic DNA and put the focus in understanding the role played by the amino-acid...
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Identifiers and source
- Literature Corpus work
- 15a70138-f70f-5f26-bb71-b6f4ef5be344
- DOI
- 10.21203/rs.3.rs-4268762/v1
