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- W2044609550 abstract "Usher syndrome is an autosomal recessive disease characterized by dual sensory impairments; affected individuals are born with a sensorineural hearing loss and ultimately lose their sight as retinitis pigmentosa develops. Conventional protein markers previously tested in a Louisiana Acadian kindred suggested tentative linkage to vitamin D-binding protein on chromosome 4. DNA linkage studies do not confirm this linkage relationship and exclude much of chromosome 4 as the site of the Usher syndrome gene in these families." @default.
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- W2044609550 date "1989-01-01" @default.
- W2044609550 modified "2023-09-27" @default.
- W2044609550 title "Exclusion of Usher syndrome gene from much of chromosome 4" @default.
- W2044609550 doi "https://doi.org/10.1159/000132733" @default.
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