[1] |
Arboleda, V. A., Lee, H., Dorrani, N., Zadeh, N., Willis, M., Macmurdo, C. F., Manning, M. A., Kwan, A., Hudgins, L., Barthelemy, F., Miceli, M. C., Quintero-Rivera, F., Kantarci, S., Strom, S. P., Deignan, J. L., Center, U. C. G., Grody, W. W., Vilain, E., Nelson, S. F., 2015. De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delay. Am. J. Hum. Genet. 96, 498-506.
|
[2] |
Armani, R., Archer, H., Clarke, A., Vasudevan, P., Zweier, C., Ho, G., Williamson, S., Cloosterman, D., Yang, N., Christodoulou, J., 2012. Transcription factor 4 and myocyte enhancer factor 2C mutations are not common causes of Rett syndrome. Am. J. Med. Genet. A. 158A, 713-719.
|
[3] |
Gold, W. A., Christodoulou, J., 2015. The utility of next-generation sequencing in gene discovery for mutation-negative patients with rett syndrome. Front. Cell. Neurosci. 9, 266.
|
[4] |
Ip, J. P. K., Mellios, N., Sur, M., 2018. Rett syndrome: insights into genetic, molecular and circuit mechanisms. Nat. Rev. Neurosci. 19, 368-382.
|
[5] |
Kaur, S., Van Bergen, N. J., Gold, W. A., Eggers, S., Lunke, S., White, S. M., Ellaway, C., Christodoulou, J., 2019. Whole exome sequencing reveals a de novo missense variant in EEF1A2 in a Rett syndrome-like patient. Clin. Case Rep. 7, 2476-2482.
|
[6] |
Kennedy, J., Goudie, D., Blair, E., Chandler, K., Joss, S., McKay, V., Green, A., Armstrong, R., Lees, M., Kamien, B., Hopper, B., Tan, T. Y., Yap, P., Stark, Z., Okamoto, N., Miyake, N., Matsumoto, N., Macnamara, E., Murphy, J. L., McCormick, E., Hakonarson, H., Falk, M. J., Li, D., Blackburn, P., Klee, E., Babovic-Vuksanovic, D., Schelley, S., Hudgins, L., Kant, S., Isidor, B., Cogne, B., Bradbury, K., Williams, M., Patel, C., Heussler, H., Duff-Farrier, C., Lakeman, P., Scurr, I., Kini, U., Elting, M., Reijnders, M., Schuurs-Hoeijmakers, J., Wafik, M., Blomhoff, A., Ruivenkamp, C. A. L., Nibbeling, E., Dingemans, A. J. M., Douine, E. D., Nelson, S. F., Study, D. D. D., Arboleda, V. A., Newbury-Ecob, R., 2019. KAT6A syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants. Genet. Med. 21, 850-860.
|
[7] |
Kong, Y., Grimaldi, M., Curtin, E., Dougherty, M., Kaufman, C., White, R. M., Zon, L. I., Liao, E. C., 2014. Neural crest development and craniofacial morphogenesis is coordinated by nitric oxide and histone acetylation. Chem. Biol. 21, 488-501.
|
[8] |
Lindeboom, R. G., Supek, F., Lehner, B., 2016. The rules and impact of nonsense-mediated mRNA decay in human cancers. Nat. Genet. 48, 1112-1118.
|
[9] |
Neul, J. L., Kaufmann, W. E., Glaze, D. G., Christodoulou, J., Clarke, A. J., Bahi-Buisson, N., Leonard, H., Bailey, M. E., Schanen, N. C., Zappella, M., Renieri, A., Huppke, P., Percy, A. K., RettSearch, C., 2010. Rett syndrome: revised diagnostic criteria and nomenclature. Ann. Neurol.. 68, 944-950.
|
[10] |
Neul, J. L., Lane, J. B., Lee, H. S., Geerts, S., Barrish, J. O., Annese, F., Baggett, L. M., Barnes, K., Skinner, S. A., Motil, K. J., Glaze, D. G., Kaufmann, W. E., Percy, A. K., 2014. Developmental delay in Rett syndrome: data from the natural history study. J. Neurodev. Disord. 6, 20.
|
[11] |
Portela, A., Esteller, M., 2010. Epigenetic modifications and human disease. Nat. Biotechnol. 28, 1057-1068.
|
[12] |
Reichow, B., George-Puskar, A., Lutz, T., Smith, I. C., Volkmar, F. R., 2015. Brief report: systematic review of Rett syndrome in males. J. Autism Dev. Disord. 45, 3377-3383.
|
[13] |
Rett, A., 1966. On a unusual brain atrophy syndrome in hyperammonemia in childhood. Wien Med. Wochenschr. 116, 723-726.
|
[14] |
Sanfeliu, A., Kaufmann, W. E., Gill, M., Guasoni, P., Tropea, D., 2019. Transcriptomic studies in mouse models of rett syndrome: a review. Neuroscience 413, 183-205.
|
[15] |
Schonewolf-Greulich, B., Bisgaard, A. M., Duno, M., Jespersgaard, C., Rokkjaer, M., Hansen, L. K., Tsoutsou, E., Sofokleous, C., Topcu, M., Kaur, S., Van Bergen, N. J., Brondum-Nielsen, K., Larsen, M. J., Sorensen, K. P., Christodoulou, J., Fagerberg, C. R., Tumer, Z., 2019a. Mosaic MECP2 variants in males with classical Rett syndrome features, including stereotypical hand movements. Clin. Genet. 95, 403-408.
|
[16] |
Schonewolf-Greulich, B., Bisgaard, A. M., Moller, R. S., Duno, M., Brondum-Nielsen, K., Kaur, S., Van Bergen, N. J., Lunke, S., Eggers, S., Jespersgaard, C., Christodoulou, J., Tumer, Z., 2019b. Clinician's guide to genes associated with Rett-like phenotypes-investigation of a Danish cohort and review of the literature. Clin. Genet. 95, 221-230.
|
[17] |
Stark, Z., Tan, T. Y., Chong, B., Brett, G. R., Yap, P., Walsh, M., Yeung, A., Peters, H., Mordaunt, D., Cowie, S., Amor, D. J., Savarirayan, R., McGillivray, G., Downie, L., Ekert, P. G., Theda, C., James, P. A., Yaplito-Lee, J., Ryan, M. M., Leventer, R. J., Creed, E., Macciocca, I., Bell, K. M., Oshlack, A., Sadedin, S., Georgeson, P., Anderson, C., Thorne, N., Melbourne Genomics Health, A., Gaff, C., White, S. M., 2016. A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders. Genet. Med. 18, 1090-1096.
|
[18] |
Tham, E., Lindstrand, A., Santani, A., Malmgren, H., Nesbitt, A., Dubbs, H. A., Zackai, E. H., Parker, M. J., Millan, F., Rosenbaum, K., Wilson, G. N., Nordgren, A., 2015. Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features. Am. J. Hum. Genet. 96, 507-513.
|
[19] |
Voss, A. K., Vanyai, H. K., Collin, C., Dixon, M. P., McLennan, T. J., Sheikh, B. N., Scambler, P., Thomas, T., 2012. MOZ regulates the Tbx1 locus, and Moz mutation partially phenocopies DiGeorge syndrome. Dev. Cell 23, 652-663.
|
[20] |
Yang, X. J., 2015. MOZ and MORF acetyltransferases: molecular interaction, animal development and human disease. Biochim. Biophys. Acta 1853, 1818-1826.
|