Identification of the Mouse Neuromuscular Degeneration Gene and Mapping of a Second Site Suppressor Allele
Open Access
- 1 December 1998
- Vol. 21 (6) , 1327-1337
- https://doi.org/10.1016/s0896-6273(00)80652-2
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Dual functions of DNA repair genes: molecular, cellular, and clinical implicationsBioEssays, 1998
- Purification and Characterization of DNA Polymerase α-Associated Replication Protein A-Dependent Yeast DNA Helicase ABiochemistry, 1997
- Genetic and Physical Maps of the Stargazer Locus on Mouse Chromosome 15Genomics, 1997
- Apoptosis: A new twist to the tale?Current Biology, 1996
- Molecular Characterization of the Rat Insulin Enhancer-binding Complex 3b2Published by Elsevier ,1995
- A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patientsNature Genetics, 1995
- Intracisternal A-type particle elements as genetic markers: detection by repeat element viral element amplified locus-PCRMammalian Genome, 1994
- The stumbler mutation maps to proximal mouse Chromosome 2Mammalian Genome, 1994
- The MEV Mouse Linkage Testing Stock: Mapping 30 Novel Proviral Insertions and Establishment of an Improved StockGenomics, 1993
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993