Behlouli, A., Bonnet, C., Abdi, S., Bouaita, A., Lelli, A., Hardelin, J., . . . Petit, C. (2014). EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness. BioMed Central.
Citação norma ChicagoBehlouli, Asma, et al. EPS8, Encoding an Actin-binding Protein of Cochlear Hair Cell Stereocilia, Is a New Causal Gene for Autosomal Recessive Profound Deafness. BioMed Central, 2014.
Citação norma MLABehlouli, Asma, et al. EPS8, Encoding an Actin-binding Protein of Cochlear Hair Cell Stereocilia, Is a New Causal Gene for Autosomal Recessive Profound Deafness. BioMed Central, 2014.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.