jmg.bmj11 天
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder ...
2 National Institute for Health Research Biomedical Research Centre, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK ...
GitHub27 天
Releases: monarch-initiative/mondo
familial acute respiratory distress syndrome, ANLN-related, dog (MONDO:1012930) neuromuscular channelopathy, KCNG1-related, cattle (MONDO:1012911) progressive retinal atrophy, FAM161A-related, dog ...