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Academic Journal

Two novel missense variants in SPTBN2 likely associated with spinocerebellar ataxia type 5.

Subjects: SPINOCEREBELLAR ataxia; MISSENSE mutation; GENETIC variationSHANDONG Sheng (China)

  • Source: Neurological Sciences; Dec2021, Vol. 42 Issue 12, p5195-5203, 9p, 1 Black and White Photograph, 2 Diagrams, 2 Charts, 1 Graph

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