A novel mouse model of CMT1B identifies hyperglycosylation as a new pathogenetic mechanism. Human molecular genetics, ddac170
The Effects of Delayed Cord Clamping on 12-Month Brain Myelin Content and Neurodevelopment: A Randomized Controlled Trial
Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy.
A mutation in the Tubb4a gene leads to microtubule accumulation with hypomyelination and demyelination
