. . . . . "NGLY1 deficiency is a novel autosomal recessive disorder of the ERAD pathway." . . . . . . . . . . . "NGLY1 deficiency is a novel autosomal recessive disorder of the endoplasmic reticulum–associated degradation pathway" . . "human - any member of Homo sapiens, unique extant species of the genus Homo" . "Tobias Kuhn" . . "RSA" . "MIGfMA0GCSqGSIb3DQEBAQUAA4GNADCBiQKBgQD4Wj537OijfOWVtsHMznuXKISqBhtGDQZfdO6pbb4hg9EHMcUFGTLbWaPrP783PHv8HMAAPjvEkHLaOHMIknqhaIa5236lfBO3r+ljVdYBElBcLvROmwG+ZGtmPNZf7lMhI15xf5TfoaSa84AFRd5J2EXekK6PhaFQhRm1IpSYtwIDAQAB" . "+FcmuPOtdFACp5JkH32lXNACrCOCFimWyGQytwnVUCjrFtNM5MKZnuE9ZeswpYDweiIV6LtWrvBkQUxCCnTCg0TeYEtckUzBmDMl/P838oa/juFexGr/oKEq9B74FnlCdE8zK8yMJMxqUtV1N9xmfTbMf6wNw8jKS+rl6Q+pkEc=" . . . "2025-04-09T06:33:41.114Z"^^ . . . . . . . . . . . . . . . . .