Exploring the clinical and epidemiological complexity ofGJB2-linked deafness

Author:

Gualandi F.,Ravani A.,Berto A.,Sensi A.,Trabanelli C.,Falciano F.,Trevisi P.,Mazzoli M.,Tibiletti M.G.,Cristofari E.,Burdo S.,Ferlini A.,Martini A.,Calzolari E.

Publisher

Wiley

Subject

Genetics (clinical)

Reference29 articles.

1. Connections with Connexins: the Molecular Basis of Direct Intercellular Signaling

2. 2001. Protocol for syndromal disorders associated with hearing impairment. In: editors. Definition, protocols and guidelines in genetic hearing impairment. London: Whurr Publishers. p 50-71.

3. 1995. Epidemiology, etiology and genetic patterns. In: editors. Hereditary hearing loss and its syndromes. Oxford: Oxford University Press. p 9-21.

4. Clinical Studies of Families With Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1)

5. A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

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