Cite
MLA Citation
Sandra Mercier et al.. “Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.” Orphanet journal of rare diseases, vol. 9, no. 1, 2014, pp. 1–16. http://access.bl.uk/ark:/81055/vdc_100080280510.0x00006c