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.
Style de citation Chicago (17e éd.)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.
Style de citation MLA (8e éd.)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.
Attention : ces citations peuvent ne pas être correctes à 100%.