📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

MOESM1 of An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids (2019)

First Author: Sundal C
Attributed to:  Understanding the genes for Parkinson's disease funded by MRC

Abstract

No abstract provided