Associated Papers
Whole exome sequencing identified three novel mutations of RTEL1 in Chinese patients with idiopathic pulmonary fibrosis.
Liu L et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease, 2025
40424856 (PubMed )
Supplement: 1-s2.0-S0925443925002728-mmc1.docx
In utero tumor development and identification of CTNNB1 mutation in a newborn case of ossifying renal tumor of infancy.
Kasai S et al.
Pediatric Blood & Cancer, 2024
38217079 (PubMed )
Supplement: supplement_1.xlsx › SNVs
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