{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n The abstract (1) provided does not include any information on the function of LINC00904. Instead, it focuses on a clinical case of the 19q13.11 microdeletion syndrome and discusses the contribution of UBA2 haploinsufficiency to the clinical phenotype. UBA2 is part of a protein complex involved in sumoylation, a post-translational modification that plays a significant role in regulating various transcription factors, hormone receptors, and signaling proteins related to brain and sexual development. As such, while the abstract contributes to our understanding of the molecular basis of this genomic disorder by highlighting the importance of UBA2, it does not offer any details regarding LINC00904.\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n (1)."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Carlos Venegas-Vega, Karem Nieto-Martínez, Alejandro Martínez-Herrera, et al. "}, {"type": "b", "children": [{"type": "t", "text": "19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cytogenet (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s13039-014-0061-z"}], "href": "https://doi.org/10.1186/s13039-014-0061-z"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25516771"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25516771"}]}]}]}