Interactions in the network of Usher syndrome type 1 proteins

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Oxford University Press

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Myosin VIIA Gene: Heterogeneity of the Mutations Responsible for Usher Syndrome Type IB

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A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

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Ala397Asp mutation of myosin VIIA gene segregating in a Spanish family with type-Ib Usher syndrome

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Localization of the Usher Syndrome Type ID Gene (Ush1D) to Chromosome 10

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