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Audiological Medicine Volume 2, 2004 - Issue 2

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Article

Guidelines and recommendations for testing of CX26 mutations and interpretation of results

Manuela Mazzoli Clock House, Lea Road, Lea, Preston, PR4ORA, UK, 612 9411 8273Correspondence[email protected]

Alessandra Murgia Clock House, Lea Road, Lea, Preston, PR4ORA, UK, 612 9411 8273

Maria Bitner Clock House, Lea Road, Lea, Preston, PR4ORA, UK, 612 9411 8273

Paulo Gasparini Clock House, Lea Road, Lea, Preston, PR4ORA, UK, 612 9411 8273

Andrew Read Clock House, Lea Road, Lea, Preston, PR4ORA, UK, 612 9411 8273

Agnete Parving Clock House, Lea Road, Lea, Preston, PR4ORA, UK, 612 9411 8273

Pages 139-140 | Published online: 11 Jul 2009

Cite this article
https://doi.org/10.1080/16513860410017359

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REFERENCES

Cryns K, Orzon E, Murgia A, Huygen P, Moreno F, et al. A genotype—phenotype correlation for GJB2 (Connexin 26) deafness. J Med Genet 2004; 41: 147—154.
PubMed Web of Science ®Google Scholar
Mazzoli M, Van Camp G, Newton V, Giabini N, Declau F. Parving A(Gendeaf): Recommendations for the Description of Genetic and Audiological Data for Families with Nonsyndromic Hereditary Hearing Impairment. Audiological Medicine 2003; 1: 148—150.
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