1. CRB1-related retinopathy overlapping the ocular phenotype of S-adenosylhomocysteine hydrolase deficiency
   Monika K. Grudzinska Pechhacker et al, 2020, Ophthalmic Genetics CrossRef
2. Lessons from animal models of endocrine disorders caused by defects of protein folding in the secretory pathway
   Yoshiaki Morishita et al, 2020, Molecular and Cellular Endocrinology CrossRef