Article
Molecular basis of classical mevalonic aciduria and the hyperimmunoglobulinaemia D and periodic fever syndrome: high frequency of 3 mutations in the mevalonate kinase gene.
Journal of inherited metabolic disease - 1 Jun 2000
Houten S M, Frenkel J, Kuis W, Wanders R J, Poll-The B T, Waterham H R
Abstract excerpt
No abstract is available from the source.
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.