A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing
Abstract Background Usher syndrome (USH) is a common heterogeneous retinopathy and a hearing loss (HL) syndrome. However, the gene causing Usher syndrome type IIC (USH2C) in a consanguineous Chinese pedigree is unknown. Methods We performed targeted next-generation sequencing analysis and Sanger seq...
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| Main Authors: | , , , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2018-06-01T00:00:00Z.
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