Cap disease uncapped, Neuromuscular Disorders, vol.17, issue.6, pp.429-461, 2007. ,
DOI : 10.1016/j.nmd.2007.03.011
"Cap disease": New congenital myopathy, Neurology, vol.31, issue.9, pp.1113-1133, 1981. ,
DOI : 10.1212/WNL.31.9.1113
???Cap disease??????a failure in the correct muscle fibre formation, Journal of the Neurological Sciences, vol.201, issue.1-2, pp.27-31, 2002. ,
DOI : 10.1016/S0022-510X(02)00156-9
???Cap myopathy???: Case report of a family, Neuromuscular Disorders, vol.16, issue.4, pp.277-81, 2006. ,
DOI : 10.1016/j.nmd.2006.01.014
Cap disease caused by heterozygous deletion of the ??-tropomyosin gene TPM2, Neuromuscular Disorders, vol.17, issue.6, pp.433-475, 2007. ,
DOI : 10.1016/j.nmd.2007.02.015
Tropomyosin isoforms: divining rods for actin cytoskeleton function, Trends in Cell Biology, vol.15, issue.6, pp.333-374, 2005. ,
DOI : 10.1016/j.tcb.2005.04.007
Vertebrate tropomyosin: distribution, properties and function, Journal of Muscle Research and Cell Motility, vol.22, issue.1, pp.5-49, 2001. ,
DOI : 10.1023/A:1010303732441
Mutations in the ??-tropomyosin (TPM2) gene ??? a rare cause of nemaline myopathy, Neuromuscular Disorders, vol.12, issue.2, pp.151-159, 2002. ,
DOI : 10.1016/S0960-8966(01)00252-8
Mutations in Genes Encoding Fast-Twitch Contractile Proteins Cause Distal Arthrogryposis Syndromes, The American Journal of Human Genetics, vol.72, issue.3, pp.681-90, 2003. ,
DOI : 10.1086/368294
A mutation in the ?? tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy, Nature Genetics, vol.328, issue.1, pp.75-84, 1995. ,
DOI : 10.1038/ng0195-75
A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: A clinical and pathological study, Neuromuscular Disorders, vol.17, issue.4, pp.330-337, 2007. ,
DOI : 10.1016/j.nmd.2007.01.017
URL : https://hal.archives-ouvertes.fr/inserm-00381952
are a common cause of congenital fiber type disproportion, Annals of Neurology, vol.102, issue.3, pp.329-366, 2008. ,
DOI : 10.1002/ana.21308
URL : https://hal.archives-ouvertes.fr/inserm-00410305
De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy, Neuromuscular Disorders, vol.12, issue.10, pp.947-51, 2002. ,
DOI : 10.1016/S0960-8966(02)00182-7
Congenital Myopathy With Nemaline Rods and Cap Structures Caused by a Mutation in the ??-Tropomyosin Gene (TPM2), Archives of Neurology, vol.64, issue.9, pp.1334-1342, 2007. ,
DOI : 10.1001/archneur.64.9.1334
Congenital myopathy with selective hypotrophy of type I fibers, Rev Neurol (Paris), vol.131, issue.11, pp.813-819, 1975. ,
Congenital Fiber Type Disproportion???30 Years On, Journal of Neuropathology & Experimental Neurology, vol.62, issue.10, pp.977-89, 2003. ,
DOI : 10.1093/jnen/62.10.977
New morphologic and genetic findings in cap disease associated with ??-tropomyosin (TPM2) mutations, Neurology, vol.71, issue.23, pp.1896-901, 2008. ,
DOI : 10.1212/01.wnl.0000336654.44814.b8
Electron micrographs of transverse sections. Peripherally located, subsarcolemal caps were clearly demarcated from neighbouring preserved myofibrils (A?C) They consisted of abnormally arranged myofibrils, containing no thick filaments (D), Bars correspond to 5 lm (A and B), 2 lm (C) and 1 lm (D) ,