Stanford Neurogenetics and Neurogenomics News & Events
- SoundCloud
NGLY1 deficiency & epilepsy
Dr Rebecca Levy of the Lucile Packard Children's Hospital in Stanford, joins the podcast to discuss her recent work looking at epilepsy in NGLY1 deficiency. Delineating the epilepsy phenotype of NGL
- DNA Science
Rare Disease Day 2023: Isla’s Story and NGLY1 Deficiency - DNA Science
The road to naming an unusual collection of unfolding symptoms is called the “diagnostic odyssey” for good reason: the journey takes, on…