Erratum: A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 (The American Journal of Human Genetics (2024) 111(1) (96–118), (S0002929723004366), (10.1016/j.ajhg.2023.12.004))
Paul MS., Michener SL., Pan H., Chan H., Pfliger JM., Rosenfeld JA., Lerma VC., Tran A., Longley MA., Lewis RA., Weisz-Hubshman M., Bekheirnia MR., Bekheirnia N., Massingham L., Zech M., Wagner M., Engels H., Cremer K., Mangold E., Peters S., Trautmann J., Perne C., Mester JL., Guillen Sacoto MJ., Person R., McDonnell PP., Cohen SR., Lusk L., Cohen ASA., Le Pichon JB., Pastinen T., Zhou D., Engleman K., Racine C., Faivre L., Moutton S., Denommé-Pichon AS., Koh HY., Poduri A., Bolton J., Knopp C., Julia Suh DS., Maier A., Toosi MB., Karimiani EG., Maroofian R., Schaefer GB., Ramakumaran V., Vasudevan P., Banos-Pinero B., Pagnamenta AT., Prasad C., Osmond M., Schuhmann S., Vasileiou G., Russ-Hall S., Scheffer IE., Carvill GL., Mefford H., Bacino CA., Lee BH., Chao (趙孝端) HT.
Main text (The American Journal of Human Genetics 111, 96–118; January 4, 2024) In the originally published version of this article there was a misalignment of columns in Table 3. This error has now been corrected in the article online. The authors regret the error.