Author:
Goldfarb Lev G.,Park Kye-Yoon,Cervenáková Larisa,Gorokhova Svetlana,Lee Hee-Suk,Vasconcelos Olavo,Nagle James W.,Semino-Mora Christina,Sivakumar Kumaraswamy,Dalakas Marinos C.
Publisher
Springer Science and Business Media LLC
Reference11 articles.
1. Fardeau, M. et al. Une nouvelle affection musculaire familiale, definie par l'accumulation intra-sarcoplasmique d'un materiel granulofilamentaire dense en microscopie electronique. Rev. Neurol. (Paris) 134, 411–425 (1978).
2. Goebel, H.H., Muller, J., Gillen, H.W. & Merritt, A.D. Autosomal dominant "spheroid body myopathy". Muscle Nerve 1, 14–26 (1978).
3. Horowitz, S.H. & Schmalbruch, H. Autosomal dominant distal myopathy with desmin storage: a clinicopathologic and electrophysiologic study of a large kinship. Muscle Nerve 17, 151– 160 (1994).
4. Goebel, H.H. Desmin-related neuromuscular disorders. Muscle Nerve 18, 1306–1320 (1995).
5. Vicart, P. et al. Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy. Hum. Genet. 98, 422–429 (1996).
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