Cite
HARVARD Citation
Bussini, A. et al. (n.d.). The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss. International journal of pediatric otorhinolaryngology. p. . [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Bussini, A. et al. (n.d.). The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss. International journal of pediatric otorhinolaryngology. p. . [Online].