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Yu HC, Coughlin CR, Geiger EA, et al. Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy. Cold Spring Harb Mol Case Stud. 2016;2(3):a000844doi: 10.1101/mcs.a000844.
Yu, H. C., Coughlin, C. R., Geiger, E. A., Salvador, B. J., Elias, E. R., Cavanaugh, J. L., Chatfield, K. C., Miyamoto, S. D., & Shaikh, T. H. (2016). Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy. Cold Spring Harbor molecular case studies, 2(3), a000844. https://doi.org/10.1101/mcs.a000844
Yu, Hung-Chun, et al. "Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy." Cold Spring Harbor molecular case studies vol. 2,3 (2016): a000844. doi: https://doi.org/10.1101/mcs.a000844
Yu HC, Coughlin CR, Geiger EA, Salvador BJ, Elias ER, Cavanaugh JL, Chatfield KC, Miyamoto SD, Shaikh TH. Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy. Cold Spring Harb Mol Case Stud. 2016 May;2(3):a000844. doi: 10.1101/mcs.a000844. PMID: 27148590; PMCID: PMC4853521.
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