FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome
Dai, H., Zhang, V.W., El‐Hattab, A.W., Ficicioglu, C., Shinawi, M., Lines, M., Schulze, A., McNutt, M., Gotway, G., Tian, X., Chen, S., Wang, J., Craigen, W.J., Wong, L.‐J.
Published in Clinical genetics (01.04.2017)
Published in Clinical genetics (01.04.2017)
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Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus
Shankar, V, Pichan, P, Eddy, RL, Jr, Tonk, V, Nowak, N, Sait, SN, Shows, TB, Schultz, RE, Gotway, G, Elkins, RC, Gilmore, MS, Sachdev, GP
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Published in American journal of respiratory cell and molecular biology (01.03.1997)
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Report of the fourth international workshop on human chromosome 15 mapping 1997
Morton, C C, Christian, S L, Donlon, T A, Driscoll, D J, Fink, J K, Gabriel, J M, Gotway, G, Greally, J M, Hitchins, M P, Howard, H C, Ji, Y, Leonard, S, Lerner, T, Magenis, E, Malcolm, S, Ohta, T, Rainier, S, Rees, M, Riley, B, Robinson, W P, Saitoh, S, Schultz, R, Sell, S, Sharp, J D, Nicholls, R D
Published in Cytogenetics and cell genetics (1999)
Published in Cytogenetics and cell genetics (1999)
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Conference Proceeding
Human and Mouse Homologs of Escherichia coli DinB (DNA Polymerase IV), Members of the UmuC/DinB Superfamily
Gerlach, Valerie L., Aravind, L., Gotway, Garrett, Schultz, Roger A., Koonin, Eugene V., Friedberg, Errol C.
Published in Proceedings of the National Academy of Sciences - PNAS (12.10.1999)
Published in Proceedings of the National Academy of Sciences - PNAS (12.10.1999)
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