Cite
HARVARD Citation
Du, H. et al. (2018). A case report of heterozygous TINF2 gene mutation associated with pulmonary fibrosis in a patient with dyskeratosis congenita. Medicine. 97 (19), p. . [Online].
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Du, H. et al. (2018). A case report of heterozygous TINF2 gene mutation associated with pulmonary fibrosis in a patient with dyskeratosis congenita. Medicine. 97 (19), p. . [Online].