APA (7th ed.) Citation

Mercier, S., Küry, S., Salort-Campana, E., Magot, A., Agbim, U., Besnard, T., . . . Bézieau, S. (2015). Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations. Orphanet journal of rare diseases, 10(1), 135. https://doi.org/10.1186/s13023-015-0352-4

Chicago Style (17th ed.) Citation

Mercier, Sandra, 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 10, no. 1 (2015): 135. https://doi.org/10.1186/s13023-015-0352-4.

MLA (9th ed.) Citation

Mercier, Sandra, 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. 10, no. 1, 2015, p. 135, https://doi.org/10.1186/s13023-015-0352-4.