CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein

This publication has 29 references indexed in Scilit:

• Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein
  Human Molecular Genetics, 2002
• A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration
  The EMBO Journal, 2000
• Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)
  Human Molecular Genetics, 1999
• Classical late infantile neuronal ceroid lipofuscinosis fibroblasts are deficient in lysosomal tripeptidyl peptidase I¹
  FEBS Letters, 1999
• CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis
  Nature Genetics, 1998
• Biosynthesis and Intracellular Targeting of the CLN3 Protein Defective in Batten Disease
  Human Molecular Genetics, 1998
• Association of Mutations in a Lysosomal Protein with Classical Late-Infantile Neuronal Ceroid Lipofuscinosis
  Science, 1997
• Isolation of a novel gene underlying batten disease, CLN3
  Cell, 1995
• Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis
  Nature, 1995
• Neuronal ceroid-lipofuscinoses in childhood
  Brain & Development, 1988