Dr Sandra Kingma from the Centre for Rare Diseases in Antwerp joins the podcast to discuss all things Mucopolysaccharidosis type I. Her recent paper asks 'where are we now?' and I asked her about where we are going next?
MPS I: Early diagnosis, bone disease and treatment, where are we now?
Sandra D. K. Kingma, An I. Jonckheere,
First published: 03 September 2021 https://doi.org/10.1002/jimd.12431
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