A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing

Overview of attention for article published in BMC Medical Genomics, June 2018

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RT @geneticcounsel: A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generatio…

A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing. https://t.co/7CsxQJtA3b https://t.co/n8ow1UOhzE

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