Associated Papers
Further Delineation of the AUTS2 HX Repeat Domain-Related Phenotype.
Erdogan EN et al.
American Journal of Medical Genetics. Part A, 2025
De novo small deletion affecting transcription start site of short isoform of AUTS2 gene in a patient with syndromic neurodevelopmental defects.
Martinez-Delgado B et al.
American Journal of Medical Genetics. Part A, 2021
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