Two novel variants in DYRK1B causative of AOMS3: expanding the clinical spectrum.
Mendoza-Caamal EC, Barajas-Olmos F, Mirzaeicheshmeh E, Ilizaliturri-Flores I, Aguilar-Salinas CA, Gómez-Velasco DV, Cicerón-Arellano I, Reséndiz-Rodríguez A, Martínez-Hernández A, Contreras-Cubas C, Islas-Andrade S, Zerrweck C, García-Ortiz H, Orozco L.
Mendoza-Caamal EC, et al. Among authors: ilizaliturri flores i.
Orphanet J Rare Dis. 2021 Jun 30;16(1):291. doi: 10.1186/s13023-021-01924-z.
Orphanet J Rare Dis. 2021.
PMID: 34193236
Free PMC article.