Shocking degeneration
Open Access
- 1 June 2004
- journal article
- editorial
- Published by Springer Nature in Nature Genetics
- Vol. 36 (6) , 547-548
- https://doi.org/10.1038/ng0604-547
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathyNature Genetics, 2004
- Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyNature Genetics, 2004
- Myofibrillar myopathy caused by novel dominant negative αB‐crystallin mutationsAnnals of Neurology, 2003
- Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21qEuropean Journal of Human Genetics, 2003
- The human genome encodes 10 α-crystallin–related small heat shock proteins: HspB1–10Cell Stress and Chaperones, 2003
- The sperm outer dense fiber protein is the 10th member of the superfamily of mammalian small stress proteinsCell Stress and Chaperones, 2003
- Alpha-B Crystallin Gene (CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in HumansAmerican Journal of Human Genetics, 2001
- A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathyNature Genetics, 1998
- Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAAHuman Molecular Genetics, 1998