Publications

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Author Title [ Year(Desc)]
Filters: Author is Novarino, Gaia and Keyword is Genetic Association Studies  [Clear All Filters]
2014
Novarino, G. et al. Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science 343, 506-511 (2014).
2018
Marin-Valencia, I. et al. A homozygous founder mutation in associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features. J Med Genet 55, 48-54 (2018).