Abstract
Survey of clinico- pathological alterations of one of well defined form of NCL family which is caused by mutation of the CLN7 protein. This protein is lokalized in lysosomes.
Its function is unknown.
Survey of clinico- pathological alterations of one of well defined form of NCL family which is caused by mutation of the CLN7 protein. This protein is lokalized in lysosomes.
Its function is unknown.