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Researchers link specific protein mutations to ataxia disease symptoms

06:41 EST 6 Nov 2019 | Science Daily

Medical researchers have linked the specific biochemical changes to a protein called CHIP to specific disease characteristics of patients with a wide range of rare disorders. The research shows it is possible to merge analyses of protein biochemistry with patient characteristics to better understand spinocerebellar ataxia autosomal recessive 16, or SCAR16.

Original Article: Researchers link specific protein mutations to ataxia disease symptoms

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