Our interest in DHTKD1 started when we set out to describe the molecular basis of 2-aminoadipic and 2-ketoadipic aciduria, an inborn error of lysine metabolism, and identified a number of novel mutations in DHTKD1. https://t.co/ElGjhw3pku
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889 followers
Just posted my first comment on #PubmedCommons. A validation of a splice mutation in our paper on DHTKD1. https://t.co/rrWNrH3CgP
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Comment on Hagen J (2015): Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria. https://t.co/Jt3KHheQoA
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Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria #DHTKD1 http://t.co/QKk5d3bDUf
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The role of #DHTKD1 in #CharcotMarieTooth disease requires further confirmation http://t.co/QKk5d3bDUf
889 followers
Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria #DHTKD1 http://t.co/QKk5d3bDUf