Items where authors include "Mullin, K."

Article

Prokopenko, D., Morgan, S.L. orcid.org/0000-0002-1734-4710, Mullin, K. et al. (9 more authors) (2021) Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. Alzheimer's & Dementia, 17 (9). pp. 1509-1527. ISSN 1552-5260

Li, A., Hooli, B., Mullin, K. et al. (7 more authors) (2017) Silencing Of The Drosophila Ortholog Of SOX5 Leads To Abnormal Neuronal Development And Behavioral Impairment. Human Molecular Genetics, 26 (8). pp. 1472-1482. ISSN 0964-6906