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Last Login: 8/6/24
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About Me: Heavy geno- and also phenotyping in 2 consanguineous family members along with CMT2 reveals HADHA as a possible unusual disease-causing gene with an intronic variant inside GDAP1 as an uncommon mutation.
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quailcamel87 1 years ago
[URL=https://www.selleckchem.com/products/tuvusertib.html]Tuvusertib[/URL]
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