rollhook69's Forum Info |
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Additional Info About rollhook69 |
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Organization associated with (JUCTCi007-A) iPSC collection from your affected individual together with congenital myasthenic syndrome (CMS) having a new homozygous mutation r.Arg331Trp (c.991C > Big t) within the CHRNE gene
https://www.selleckchem.com/products/sbe-b-cd.html |
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