APA

Turunen J. A., Wedenoja J., Repo P., Järvinen R., Jäntti J. E., Mörtenhumer S., Riikonen A. S., Lehesjoki A., Majander A. & Kivelä T. T. (20181211). Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene. : American journal of ophthalmology.

Chicago

Turunen Joni A, Wedenoja Juho, Repo Pauliina, Järvinen Reetta-Stiina, Jäntti Johannes E, Mörtenhumer Sanna, Riikonen Antti S, Lehesjoki Anna-Elina, Majander Anna and Kivelä Tero T. 20181211. Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene. : American journal of ophthalmology.

Harvard

Turunen J. A., Wedenoja J., Repo P., Järvinen R., Jäntti J. E., Mörtenhumer S., Riikonen A. S., Lehesjoki A., Majander A. and Kivelä T. T. (20181211). Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene. : American journal of ophthalmology.

MLA

Turunen Joni A, Wedenoja Juho, Repo Pauliina, Järvinen Reetta-Stiina, Jäntti Johannes E, Mörtenhumer Sanna, Riikonen Antti S, Lehesjoki Anna-Elina, Majander Anna and Kivelä Tero T. Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene. : American journal of ophthalmology. 20181211.