Cofactor role for 10-formyldihydrofolic acid.

Por Baggott, J E, Johanning, G L, Branham, K E, Prince, C W, Morgan, S L, Eto, I, Vaughn, W H
Publicado em 1995

exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels

Por Maranhao, B., Biswas, P., Duncan, J.L., Branham, K.E., Silva, G.A., Naeem, M.A., Khan, S.N., Riazuddin, S., Hejtmancik, J.F., Heckenlively, J.R., Riazuddin, S.A., Lee, P.L., Ayyagari, R.
Publicado em 2014