D. Kurz

Transient N‐glycosylation abnormalities likely due to a de novo loss‐of‐function mutation in the delta subunit of coat protein I

T. Marquardt, R. Fingerhut, S. Rust, 2019, American journal of medical genetics. Part A.

11-cis retinol dehydrogenase mutations as a major cause of the congenital night-blindness disorder known as fundus albipunctatus.

D. Han, F. Gonzalez-fernandez, S. Newman, 1999, Molecular vision.

Comparative gene identification 58/α/β hydrolase domain 5 lacks lysophosphatidic acid acyltransferase activity

G. Carman, D. Brasaemle, G. Han, 2014, Journal of Lipid Research.