Bork, J. M., Peters, L. M., Riazuddin, S., Bernstein, S. L., Ahmed, Z. M., Ness, S. L., . . . Morell, R. J. (2001). Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23. The American Society of Human Genetics.
Citação norma ChicagoBork, Julie M., et al. Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused By Allelic Mutations of the Novel Cadherin-Like Gene CDH23. The American Society of Human Genetics, 2001.
Citação norma MLABork, Julie M., et al. Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused By Allelic Mutations of the Novel Cadherin-Like Gene CDH23. The American Society of Human Genetics, 2001.