Subject
Clinical Neurology,Neurology
Reference62 articles.
1. Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V;Antonellis;Am J Hum Genet,2003
2. Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V: a clinical, electrophysiological and genetic study;Auer-Grumbach;Brain,2000
3. Phenotypes of the N88S Berardinelli-Seip congenital lipodystrophy 2 mutation;Auer-Grumbach;Ann Neurol,2005
4. Bertini E, Gadisseux JL, Palmieri G, Ricci E, Di Capua M, Ferriere G, et al. Distal infantile spinal muscularatrophy associated with paralysis of the diaphragm: a variant of infantilespinal muscular atrophy. Am J Med Genet 1989;33:328–35.
5. Sur une forme particulière d’atrophie musculaire progressive, souvent familiale, débutant par les pieds et les jambes et atteignant plus tard les mains;Charcot;Rev Med,1886
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