{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nThe provided abstract (1) focused on elucidating genetic causes of premature ovarian insufficiency through whole exome sequencing and subsequent identification of candidate variants in genes central to DNA damage repair and meiosis—for example, REC8 and HROB—as well as other factors such as MCM8, NUP107, STAG3, HFM1, and POF1B. Notably, the long non‐coding transcript HECW1‐IT1 was not specifically mentioned or functionally described in the study. Thus, based on this abstract, no functional insights regarding HECW1‐IT1 are available, and its role in ovarian physiology or pathogenesis remains to be elucidated by future research."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Elena J Tucker, Katrina M Bell, Gorjana Robevska, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Hum Genet (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41431-021-00977-9"}], "href": "https://doi.org/10.1038/s41431-021-00977-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34707299"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34707299"}]}]}]}