Riazuddin, S., Belyantseva, I. A., Giese, A., Lee, K., Indzhykulian, A. A., Nandamuri, S. P., . . . Ahmed, Z. M. (2012). Mutations in CIB2, a calcium and integrin binding protein, cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
Styl cytowania ChicagoRiazuddin, Saima, et al. Mutations in CIB2, a Calcium and Integrin Binding Protein, Cause Usher Syndrome Type 1J and Nonsyndromic Deafness DFNB48. 2012.
Styl cytowania MLARiazuddin, Saima, et al. Mutations in CIB2, a Calcium and Integrin Binding Protein, Cause Usher Syndrome Type 1J and Nonsyndromic Deafness DFNB48. 2012.
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