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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
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; Undiagnosed Diseases Network; Bacino CA, Lee BH, Chao 趙孝端 HT. Paul MS, et al. Among authors: pan h. Am J Hum Genet. 2024 May 8:S0002-9297(24)00163-0. doi: 10.1016/j.ajhg.2024.04.022. Online ahead of print. Am J Hum Genet. 2024. PMID: 38723631 No abstract available.
Spin disorder control of topological spin texture.
Zhang H, Shao YT, Chen X, Zhang B, Wang T, Meng F, Xu K, Meisenheimer P, Chen X, Huang X, Behera P, Husain S, Zhu T, Pan H, Jia Y, Settineri N, Giles-Donovan N, He Z, Scholl A, N'Diaye A, Shafer P, Raja A, Xu C, Martin LW, Crommie MF, Yao J, Qiu Z, Majumdar A, Bellaiche L, Muller DA, Birgeneau RJ, Ramesh R. Zhang H, et al. Among authors: pan h. Nat Commun. 2024 May 7;15(1):3828. doi: 10.1038/s41467-024-47715-5. Nat Commun. 2024. PMID: 38714653 Free PMC article.
9,382 results