Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm
Onoufriadis, A., Shoemark, A., Munye, M. M., James, C. T., Schmidts, M., Patel, M., Rosser, E. M., Bacchelli, C., Beales, P. L., Scambler, P. J., Hart, S. L., Danke-Roelse, J. E., Sloper, J. J., Hull,Том:
51
Мова:
english
Журнал:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2013-101938
Date:
January, 2014
Файл:
PDF, 8.34 MB
english, 2014
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