Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16
- 1 October 1990
- Vol. 8 (2) , 387-390
- https://doi.org/10.1016/0888-7543(90)90297-8
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Infantile neuronal ceroid-lipofuscinosis is not an allelic form of batten disease: Exclusion of chromosome 16 region with linkage analysesGenomics, 1990
- A primary map of 24 loci on human chromosome 16Genomics, 1990
- Batten disease (Spielmeyer‐Sjogren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16Clinical Genetics, 1989
- Ovine Ceroid LipofuscinosisJournal of Biological Chemistry, 1989
- Palcental pathology and prenatal diagnosis of infantile type of neuronal ceroid-lipofuscinosisAmerican Journal of Medical Genetics, 1988
- Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1 ? q22.3 in a patient with tyrosinemia type IIHuman Genetics, 1987
- Prenatal diagnosis of neuronal ceroid‐lipofuscinosesAmerican Journal of Medical Genetics, 1985
- Localization of the haptoglobin α and β genes (HPA and HPB) to human chromosome 16q22 by in situ hybridizationCytogenetic and Genome Research, 1984
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- Sequence of human haptoglobin cDNA: evidence that the α and β subunits are coded by the same mRNANucleic Acids Research, 1983