Publisher
Springer Science and Business Media LLC
Reference31 articles.
1. Skre H (1974) Genetic and clinical aspects of Charcot-Marie-Tooth’s disease. Clin Genet 6:98–118
2. Dyck PJ, Chance P, Lebo R, Carney JA (1994) Hereditary motor and sensory neuropathies. In: Dyck PJ, Thomas PK, Griffin JW, Low PA and Poduslo JF (Eds.), Peripheral Neuropathy, 3rd edn., W.B. Saunders Co., Philadelphia, PA, pp 1094–1136.
3. Bombelli F, Stojkovic T, Dubourg O, Echaniz-Laguna A, Tardieu S et al (2014) Charcot-Marie-Tooth disease type 2A: from typical to rare phenotypic and genotypic features. JAMA Neurol 71:1036–1042
4. Verhoeven K, Claeys KG, Züchner S, Schröder JM, Weis J, CeutericK C et al (2006) MFN2 mutation distribution and genotype/ phenotype correlation in Charcot-Marie-Tooth type 2. Brain 129:2093–2102
5. Di Meglio C, Bonello-Palot N, Boulay C, Milh M, Ovaert C, Levy N, Chabrol B (2016) Clinical and allelic heterogeneity in a pediatric cohort of 11 patients carrying MFN2 mutation. Brain Dev 38:498–506
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献