APA
Mao D., Reuter C. M., Ruzhnikov M. R. Z., Beck A. E., Farrow E. G., Emrick L. T., Rosenfeld J. A., Mackenzie K. M., Robak L., Wheeler M. T., Burrage L. C., Jain M., Liu P., Calame D., Küry S., Sillesen M., Schmitz-Abe K., Tonduti D., Spaccini L., Iascone M., Genetti C. A., Koenig M. K., Graf M., Tran A., Alejandro M., Lee B. H., Thiffault I., Agrawal P. B., Bernstein J. A., Bellen H. J. & Chao H. (20200511). De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation. : American journal of human genetics.
Chicago
Mao Dongxue, Reuter Chloe M, Ruzhnikov Maura R Z, Beck Anita E, Farrow Emily G, Emrick Lisa T, Rosenfeld Jill A, Mackenzie Katherine M, Robak Laurie, Wheeler Matthew T, Burrage Lindsay C, Jain Mahim, Liu Pengfei, Calame Daniel, Küry Sébastien, Sillesen Martin, Schmitz-Abe Klaus, Tonduti Davide, Spaccini Luigina, Iascone Maria, Genetti Casie A, Koenig Mary K, Graf Madeline, Tran Alyssa, Alejandro Mercedes, Lee Brendan H, Thiffault Isabelle, Agrawal Pankaj B, Bernstein Jonathan A, Bellen Hugo J and Chao Hsiao-Tuan. 20200511. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation. : American journal of human genetics.
Harvard
Mao D., Reuter C. M., Ruzhnikov M. R. Z., Beck A. E., Farrow E. G., Emrick L. T., Rosenfeld J. A., Mackenzie K. M., Robak L., Wheeler M. T., Burrage L. C., Jain M., Liu P., Calame D., Küry S., Sillesen M., Schmitz-Abe K., Tonduti D., Spaccini L., Iascone M., Genetti C. A., Koenig M. K., Graf M., Tran A., Alejandro M., Lee B. H., Thiffault I., Agrawal P. B., Bernstein J. A., Bellen H. J. and Chao H. (20200511). De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation. : American journal of human genetics.
MLA
Mao Dongxue, Reuter Chloe M, Ruzhnikov Maura R Z, Beck Anita E, Farrow Emily G, Emrick Lisa T, Rosenfeld Jill A, Mackenzie Katherine M, Robak Laurie, Wheeler Matthew T, Burrage Lindsay C, Jain Mahim, Liu Pengfei, Calame Daniel, Küry Sébastien, Sillesen Martin, Schmitz-Abe Klaus, Tonduti Davide, Spaccini Luigina, Iascone Maria, Genetti Casie A, Koenig Mary K, Graf Madeline, Tran Alyssa, Alejandro Mercedes, Lee Brendan H, Thiffault Isabelle, Agrawal Pankaj B, Bernstein Jonathan A, Bellen Hugo J and Chao Hsiao-Tuan. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation. : American journal of human genetics. 20200511.