Concepedia
Clinica Chimica Acta · 1999 · 33 citations · 11 references
Life SciencesNeurologyPathologyClinical BiochemistryEnzymologyNeuropathologyClinical EnzymologyLysosomal BiochemistryLysosomal DysfunctionLysosomal Storage DisordersPediatric NeuropathologyAssay
11
Association of Mutations in a Lysosomal Protein with Classical Late-Infantile Neuronal Ceroid Lipofuscinosis
David E. Sleat, Robert Donnelly, Henry Lackland et al. · Science · 1997 · 583 citations
Life Sciences, Genetics, Neuroscience +15
Mitochondrial ATP synthase subunit <i>c</i> storage in the ceroid‐lipofuscinoses (Batten disease)
David N. Palmer, Ian M. Fearnley, John E. Walker et al. · American Journal of Medical Genetics · 1992 · 365 citations
Life Sciences, Biochemistry, Molecular Biology +15
Synthesis and chemistry of 7-amino-4-(trifluoromethyl)coumarin and its amino acid and peptide derivatives
Eugene R. Bissell, Alexander R. Mitchell, Robert E. Smith · The Journal of Organic Chemistry · 1980 · 89 citations
Natural Sciences, Chemistry, Medicinal Chemistry +8
Purification and properties of a pepstatin-insensitive carboxyl proteinase from a Gram-negative bacterium
Kōhei Oda, Masafumi Sugitani, Ken-ichi Fukuhara et al. · Biochimica et Biophysica Acta (BBA) - General Subjects · 1987 · 66 citations
Life Sciences, Biochemistry, Microbiology +13
Structural Organization and Sequence ofCLN2,the Defective Gene in Classical Late Infantile Neuronal Ceroid Lipofuscinosis
Chang‐Gong Liu, David E. Sleat, Robert Donnelly et al. · Genomics · 1998 · 63 citations
Life Sciences, Genetics, Neuroscience +4