Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein

Adam Chamberlin, Robert Huether, Aline Z. Machado, Michael Groden, Hsiao Mei Liu, Kinnari Upadhyay, Vivian O, Nathalia L. Gomes, Antonio M. Lerario, Mirian Y. Nishi, Elaine M.F. Costa, Berenice Mendonca, Sorahia Domenice, Jacqueline Velasco, Johnny C. Loke, Harry Ostrer

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)1620-1628
Number of pages9
JournalHuman molecular genetics
Volume28
Issue number10
DOIs
StatePublished - May 15 2019

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Chamberlin, A., Huether, R., Machado, A. Z., Groden, M., Liu, H. M., Upadhyay, K., O, V., Gomes, N. L., Lerario, A. M., Nishi, M. Y., Costa, E. M. F., Mendonca, B., Domenice, S., Velasco, J., Loke, J. C., & Ostrer, H. (2019). Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein. Human molecular genetics, 28(10), 1620-1628. https://doi.org/10.1093/hmg/ddz002