Non-Syndromic Hearing Loss and High-Throughput Strategies to Decipher Its Genetic Heterogeneity

Author:

Zhong Liu Xue,Kun Shan,Jing Qing,Jing Cheng,Denise Yan

Publisher

Elsevier BV

Subject

Otorhinolaryngology

Reference157 articles.

1. Mutations of MYO6 are associated with recessive deafness, DFNB37;Ahmed;Am. J. Hum. Genet.,2003

2. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23;Ahmed;Hum. Molec. Genet.,2003

3. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations;Albert;European Journal of Human Genetics,2006

4. The genetic bases for syndromic and nonsyndromic deafness among Jews;Ben-Yosef;Trends Mol Med,2001

5. Hereditary deafness and phenotyping in humans;Bitner-Glindzicz;Br Med Bull.,2002

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