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
ZCCHC8 p.P410A disrupts nucleocytoplasmic localization, promoting idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease.
Wang CY et al.
Molecular Medicine (cambridge, Mass.), 2024
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