APA
Nguyen T. T. M., Murakami Y., Sheridan E., Ehresmann S., Rousseau J., St-Denis A., Chai G., Ajeawung N. F., Fairbrother L., Reimschisel T., Bateman A., Berry-Kravis E., Xia F., Tardif J., Parry D. A., Logan C. V., Diggle C., Bennett C. P., Hattingh L., Rosenfeld J. A., Perry M. S., Parker M. J., Le Deist F., Zaki M. S., Ignatius E., Isohanni P., Lönnqvist T., Carroll C. J., Johnson C. A., Gleeson J. G., Kinoshita T. & Campeau P. M. (20171113). Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia. : American journal of human genetics.
Chicago
Nguyen Thi Tuyet Mai, Murakami Yoshiko, Sheridan Eamonn, Ehresmann Sophie, Rousseau Justine, St-Denis Anik, Chai Guoliang, Ajeawung Norbert F, Fairbrother Laura, Reimschisel Tyler, Bateman Alexandra, Berry-Kravis Elizabeth, Xia Fan, Tardif Jessica, Parry David A, Logan Clare V, Diggle Christine, Bennett Christopher P, Hattingh Louise, Rosenfeld Jill A, Perry Michael Scott, Parker Michael J, Le Deist Françoise, Zaki Maha S, Ignatius Erika, Isohanni Pirjo, Lönnqvist Tuula, Carroll Christopher J, Johnson Colin A, Gleeson Joseph G, Kinoshita Taroh and Campeau Philippe M. 20171113. Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia. : American journal of human genetics.
Harvard
Nguyen T. T. M., Murakami Y., Sheridan E., Ehresmann S., Rousseau J., St-Denis A., Chai G., Ajeawung N. F., Fairbrother L., Reimschisel T., Bateman A., Berry-Kravis E., Xia F., Tardif J., Parry D. A., Logan C. V., Diggle C., Bennett C. P., Hattingh L., Rosenfeld J. A., Perry M. S., Parker M. J., Le Deist F., Zaki M. S., Ignatius E., Isohanni P., Lönnqvist T., Carroll C. J., Johnson C. A., Gleeson J. G., Kinoshita T. and Campeau P. M. (20171113). Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia. : American journal of human genetics.
MLA
Nguyen Thi Tuyet Mai, Murakami Yoshiko, Sheridan Eamonn, Ehresmann Sophie, Rousseau Justine, St-Denis Anik, Chai Guoliang, Ajeawung Norbert F, Fairbrother Laura, Reimschisel Tyler, Bateman Alexandra, Berry-Kravis Elizabeth, Xia Fan, Tardif Jessica, Parry David A, Logan Clare V, Diggle Christine, Bennett Christopher P, Hattingh Louise, Rosenfeld Jill A, Perry Michael Scott, Parker Michael J, Le Deist Françoise, Zaki Maha S, Ignatius Erika, Isohanni Pirjo, Lönnqvist Tuula, Carroll Christopher J, Johnson Colin A, Gleeson Joseph G, Kinoshita Taroh and Campeau Philippe M. Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia. : American journal of human genetics. 20171113.