Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children
β Scribed by Xiangyang Hu; Fenghe Liang; Min Zhao; Angela Gong; Emily R. Berry; Yang Shi; Yanxiao Wang; Yan Chen; Aishu Liu; Chunyan Qu
- Book ID
- 118454468
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 360 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0165-5876
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Pendred syndrome is an autosomal-recessive disorder characterized by congenital sensorineural hearing loss combined with goiter. This disorder may account for up to 10% of cases of hereditary deafness. The disease gene ( PDS/SLC26A4) has been mapped to chromosome 7q22-q31 and encodes a chloride-iodi
Pendred syndrome is an autosomal-recessive disorder characterized by congenital sensorineural hearing loss combined with goiter. This disorder may account for up to 10% of cases of hereditary deafness. The disease gene (PDS/SLC26A4) has been mapped to chromosome 7q22-q31 and encodes a chloride-iodid