Booth, K. T., Kahrizi, K., Najmabadi, H., Azaiez, H., & Smith, R. J. (2018). Old gene, new phenotype: Splicing altering variants in CEACAM16 cause recessive non-syndromic hearing impairment. J Med Genet.

Booth, Kevin T., Kimia Kahrizi, Hossein Najmabadi, Hela Azaiez, και Richard J. Smith. "Old Gene, New Phenotype: Splicing Altering Variants in CEACAM16 Cause Recessive Non-syndromic Hearing Impairment." J Med Genet 2018.

Booth, Kevin T., et al. "Old Gene, New Phenotype: Splicing Altering Variants in CEACAM16 Cause Recessive Non-syndromic Hearing Impairment." J Med Genet 2018.