A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss

MLA

Primignani, P., et al. “A Novel Dominant Missense Mutation--D179N--in the GJB2 Gene (Connexin 26) Associated with Non-Syndromic Hearing Loss.” Clinical Genetics, vol. 63, no. 6, June 2003. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.pmid.dedup....c2ce6436dbbda2f56f7dfaed3bedecb6&authtype=sso&custid=ns315887.

APA

Primignani, P., Castorina, P., Sironi, F., Curcio, C., Ambrosetti, U., & Coviello, D. (2003). A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss. Clinical Genetics, 63(6).

Chicago

Primignani, P, P Castorina, F Sironi, C Curcio, U Ambrosetti, and Domenico Coviello. 2003. “A Novel Dominant Missense Mutation--D179N--in the GJB2 Gene (Connexin 26) Associated with Non-Syndromic Hearing Loss.” Clinical Genetics 63 (6). http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.pmid.dedup....c2ce6436dbbda2f56f7dfaed3bedecb6&authtype=sso&custid=ns315887.