TY  - RPRT
TI  - Synonymous SNP: Rare versus frequent codon can cause Phenotypic changes in the human genome
AU  - SRIVASTAV, A.
PY  - 2019
DO  - 10.1101/582213
UR  - https://www.biorxiv.org/content/10.1101/582213v1
ID  - 10.1101/582213
ER  -