MYH2-associated myopathy caused by novel compound heterozygous mutations: a case report and literature review
Morales PN, Coons AN, Koopman AJ, Patel S, Chase PB, Parvatiyar MS, et al. Post-translational modifications of vertebrate…
Machine learning in Alzheimer’s disease genetics
School of Medicine, Cardiff University, Cardiff, UK Matthew Bracher-Smith, Julie Williams, Nicola Denning, Alun Meggy & Valentina Escott-Price Centre for Neuropsychiatric Genetics and…