Infantile neuronal ceroid-lipofuscinosis is not an allelic form of batten disease: Exclusion of chromosome 16 region with linkage analyses
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference14 articles.
1. Batten disease (Spielmeyer-Sjögren disease) and haptoglobins (HP): Indication of linkage and assignment to chromosome 16;Eiberg;Clin. Genet.,1989
2. Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid lipofuscinosis) gene (CLN3) maps to human chromosome 16;Gardiner;Genomics,1990
3. High-mannose dolichol-linked oligosaccharides in infantile ceroid lipofuscinosis;Hall;Biochem. Soc. Trans.,1989
4. Human Gene Mapping 10;Cytogenet. Cell Genet.,1989
5. Restriction fragment length polymorphisms detected by anonymous DNA probes mapped to defined intervals of human chromosome 16;Hyland;Hum. Genet.,1988
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1. Bioinformatic perspectives in the neuronal ceroid lipofuscinoses;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2013-11
2. Pirkko Santavuori (1933-2004);Journal of Child Neurology;2004-06
3. Specific Delay in the Degradation of Mitochondrial ATP Synthase Subunit c in Late Infantile Neuronal Ceroid Lipofuscinosis Is Derived from Cellular Proteolytic Dysfunction Rather than Structural Alteration of Subunit c;Journal of Neurochemistry;2002-11-23
4. Bibliography on ceroid-lipofuscinoses, II;American Journal of Medical Genetics;1995-06
5. Refined Assignment of the Infantile Neuronal Ceroid Lipofuscinosis (INCL, CLN1) Locus at 1p32: Incorporation of Linkage Disequilibrium in Multipoint Analysis;Genomics;1993-06
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