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Pathogenetic role of the deafness-related M34T mutation of Cx26.
Bicego M, Beltramello M, Melchionda S, Carella M, Piazza V, Zelante L, Bukauskas FF, Arslan E, Cama E, Pantano S, Bruzzone R, D'Andrea P, Mammano F. Bicego M, et al. Among authors: cama e. Hum Mol Genet. 2006 Sep 1;15(17):2569-87. doi: 10.1093/hmg/ddl184. Epub 2006 Jul 18. Hum Mol Genet. 2006. PMID: 16849369 Free PMC article.
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian family.
Alemanno MS, Cama E, Santarelli R, Carella M, Zelante L, Toffolatti L, Palladino T, Melchionda S, Arslan E. Alemanno MS, et al. Among authors: cama e. Int J Pediatr Otorhinolaryngol. 2009 Jan;73(1):127-31. doi: 10.1016/j.ijporl.2008.09.019. Epub 2008 Nov 5. Int J Pediatr Otorhinolaryngol. 2009. PMID: 18990456
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation.
Santarelli R, Rossi R, Scimemi P, Cama E, Valentino ML, La Morgia C, Caporali L, Liguori R, Magnavita V, Monteleone A, Biscaro A, Arslan E, Carelli V. Santarelli R, et al. Among authors: cama e. Brain. 2015 Mar;138(Pt 3):563-76. doi: 10.1093/brain/awu378. Epub 2015 Jan 5. Brain. 2015. PMID: 25564500 Free PMC article.
84 results