K93n Na1 Kansai Chiharu 118 Free [work] -

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The K93N mutation (sometimes written as p.Lys93Asn) has also been documented in human genes like SORBS3 and FBXL22 . In the SORBS3 gene, it is considered a variant of "uncertain significance". Meanwhile, a mutation in the FBXL22 gene, which is involved in sarcomere physiology (muscle function), has been flagged as a candidate for pathogenicity. k93n na1 kansai chiharu 118 free

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