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.
Chicago Style (17th ed.) CitationKhan, 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.
MLA (8th ed.) CitationKhan, 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.
Warning: These citations may not always be 100% accurate.