Myelin genes: getting the dosage right
- 1 November 1995
- journal article
- editorial
- Published by Springer Nature in Nature Genetics
- Vol. 11 (3) , 226-228
- https://doi.org/10.1038/ng1195-226
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient miceNature Genetics, 1995
- Protein zero (P0)–deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathiesNature Genetics, 1995
- Biology and Genetics of Hereditary Motor and Sensory NeuropathiesAnnual Review of Neuroscience, 1995
- Charcot-Marie-tooth disease: a new paradigm for the mechanism of inherited diseaseTrends in Genetics, 1994
- Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transportJournal of Neuroscience Research, 1994
- X–linked spastic paraplegia and Pelizaeus–Merzbacher disease are allelic disorders at the proteolipid protein locusNature Genetics, 1994
- Nerve conduction studies in Charcot‐Marie‐Tooth polyneuropathy associated with a segmental duplication of chromosome 17Neurology, 1993
- Comparison of Trembler and Trembler-J Mouse PhenotypesJournal of Neuropathology and Experimental Neurology, 1983
- Hereditary demyelinating neuropathy in the Trembler mouseJournal of the Neurological Sciences, 1975