Author

Ramya Ranganathan

University of SheffieldORCID 0000-0001-7861-2646Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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2022-2022 · peak 1/yr

9 top collaborators · 36 mutual co-author links

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1 shared paperNeuroscience

Adrian Higginbottom

Mutual co-authors in cluster

1 paper

NeurosciencebioRxivPreprintJun 28, 2022

This paper identifies GLT8D1 mutations as a cause of ALS by disrupting neurotrophin signaling in lipid rafts through reduced ganglioside expression.

3 citations