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FUNCTIONAL INVESTIGATION F337C MUTATION IN THE CLCN1 GENE ASSOCIATED WITH
PRINCIPAL MYOTONIA CONGENITA SHOWS

 * Post author By admin
 * Post date July 30, 2023
 * No Comments on Functional investigation F337C mutation in the CLCN1 gene
   associated with principal myotonia congenita shows

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← Mixing phage exhibit using SMRTbell next-generation sequencing for the fast
breakthrough discovery involving functional scFv broken phrases.

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