Settling the myelin protein zero question in CMT1B
- 1 October 1995
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 11 (2) , 119-120
- https://doi.org/10.1038/ng1095-119
Abstract
No abstract availableKeywords
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- Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot–Marie–Tooth disease type 1BNature Genetics, 1993
- Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneNature Genetics, 1993
- Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene regionHuman Genetics, 1991