Bronwyn Grinton

3PUBLICATIONS
19CO-AUTHORS
Aboriginal and Torres Strait Islander artefactsNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
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Publications (3)

|Sep 18, 2026
SLC7A6OS Founder Mutation: A Rare Cause of Progressive Myoclonus Epilepsy Dated to 1100 Years Ago.

|Apr 11, 2023
Recognition and epileptology of protracted CLN3 disease.

Jillian M Cameron, John A Damiano, Bronwyn Grinton

|Feb 22, 2023
Genes4Epilepsy: An epilepsy gene resource.

Karen L Oliver, Ingrid E Scheffer, Mark F Bennett

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