Hereditary Motor and Sensory Neuropathy Mutation
References
- Hoogendijk JE Hensels GW Gabreels-Festen AA Gabreels FJ Janssen EA de Jonghe P De-novo mutation in hereditary motor and sensory neuropathy type I Lancet 1992 May 2 339 8801 1081 1082 10.1016/0140-6736(92)90668-S 1349106
- Hallam PJ Harding AE Berciano J Barker DF Malcolm S Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1) Ann Neurol 1992 May 31 5 570 572 10.1002/ana.410310518 1596093
- Ionasescu VV Trofatter J Haines JL Ionasescu R Searby C Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy Neurology 1992 Apr 42 4 903 908 10.1212/WNL.42.4.903 1565250
DOI: https://doi.org/10.15844/pedneurbriefs-6-6-5 | Journal eISSN: 2166-6482
Language: English
Page range: 44 - 44
Published on: Jun 1, 1992
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
Keywords:
© 1992 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.