APA citiranje

Eisenberger, T., Slim, R., Mansour, A., Nauck, M., Nürnberg, G., Nürnberg, P., . . . Bolz, H. J. (2012). Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3. BioMed Central.

Citação norma Chicago

Eisenberger, Tobias, et al. Targeted Next-generation Sequencing Identifies a Homozygous Nonsense Mutation in ABHD12, the Gene Underlying PHARC, in a Family Clinically Diagnosed With Usher Syndrome Type 3. BioMed Central, 2012.

MLA citiranje

Eisenberger, Tobias, et al. Targeted Next-generation Sequencing Identifies a Homozygous Nonsense Mutation in ABHD12, the Gene Underlying PHARC, in a Family Clinically Diagnosed With Usher Syndrome Type 3. BioMed Central, 2012.