Dominant Hereditary Inclusion-Body Myopathy Gene (IBM3) Maps to Chromosome Region 17p13.1
- 1 May 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (5) , 1420-1426
- https://doi.org/10.1086/302375
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in RecombinationAmerican Journal of Human Genetics, 1998
- Assignment of the Tibial Muscular Dystrophy Locus to Chromosome 2q31American Journal of Human Genetics, 1998
- A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyNature Genetics, 1995
- A Comprehensive Human Linkage Map with Centimorgan DensityScience, 1994
- Five skeletal myosin heavy chain genes are organized as a multigene complex in the human genomeHuman Molecular Genetics, 1993
- Co-expression of multiple myosin heavy chain genes, in addition to a tissue-specific one, in extraocular musculature.The Journal of cell biology, 1985
- Multigene Family for Sarcomeric Myosin Heavy Chain in Mouse and Human DNA: Localization on a Single ChromosomeScience, 1983
- Oculopharyngeal muscular dystrophy and distal myopathyActa Neurologica Scandinavica, 1982
- Three myosin heavy-chain isozymes appear sequentially in rat muscle developmentNature, 1981
- Rimmed vacuolesActa Neuropathologica, 1980