Cite
HARVARD Citation
del Castillo, F. et al. (2005). A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment. Journal of medical genetics. 42 (7), pp. 588-594. [Online].