Cita APA (7a ed.)

Khan, A. O., Becirovic, E., Betz, C., Neuhaus, C., Altmüller, J., Riedmayr, L. M., . . . Bolz, H. J. (2017). A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian Peninsula. Nature Portfolio.

Cita Chicago Style (17a ed.)

Khan, Arif O., et al. A Deep Intronic CLRN1 (USH3A) Founder Mutation Generates an Aberrant Exon and Underlies Severe Usher Syndrome on the Arabian Peninsula. Nature Portfolio, 2017.

Cita MLA (8a ed.)

Khan, Arif O., et al. A Deep Intronic CLRN1 (USH3A) Founder Mutation Generates an Aberrant Exon and Underlies Severe Usher Syndrome on the Arabian Peninsula. Nature Portfolio, 2017.