We report a Belgian family with autosomal dominant, late-onset, distal myopathy with selective foot extensor muscle involvement of the lower legs. Linkage to the tibial muscular dystrophy (TMD) locus 2q31 was not evident at first because of incomplete disease penetrance in a 50-year-old asymptomatic family member. An abnormal tibialis anterior muscle biopsy established her subclinical status and linkage of the family to the TMD locus. Mutation analysis showed a disease-specific, heterozygous point mutation in the last exon, Mex6, of the titin gene. This is the third mutation found in TMD and the second European family with TMD outside the Finnish population, suggesting that titinopathies may occur in various populations
Tibial muscular dystrophy (TMD) is the first described human titinopathy. It is a mild adult-onset s...
Mutations in the gene encoding the giant skeletal muscle protein titin are associated with a variety...
International audienceBackground and purposeThe aim was to determine the genetic background of unkno...
Tibial muscular dystrophy (TMD) or Udd myopathy is an autosomal dominant distal myopathy with late o...
SummaryTibial muscular dystrophy (TMD) is a rare autosomal dominant distal myopathy with late adult ...
International audienceSeveral patients with previously reported titin gene (TTN) mutations causing t...
Tibial muscular dystrophy (TMD) is an autosomal dominant late-onset distal myopathy linked to chromo...
Tibial muscular dystrophy (TMD) is an autosomal dominant late-onset distal myopathy linked to chromo...
ABSTRACT A study on tibial muscular dystrophy (TMD) in a selected patient group in Oslo TMD is an a...
Tibial muscular dystrophy (TMD) is the first described human titinopathy. It is a mild adult-onset s...
Mutations in the gene encoding the giant skeletal muscle protein titin are associated with a variety...
International audienceBackground and purposeThe aim was to determine the genetic background of unkno...
Tibial muscular dystrophy (TMD) or Udd myopathy is an autosomal dominant distal myopathy with late o...
SummaryTibial muscular dystrophy (TMD) is a rare autosomal dominant distal myopathy with late adult ...
International audienceSeveral patients with previously reported titin gene (TTN) mutations causing t...
Tibial muscular dystrophy (TMD) is an autosomal dominant late-onset distal myopathy linked to chromo...
Tibial muscular dystrophy (TMD) is an autosomal dominant late-onset distal myopathy linked to chromo...
ABSTRACT A study on tibial muscular dystrophy (TMD) in a selected patient group in Oslo TMD is an a...
Tibial muscular dystrophy (TMD) is the first described human titinopathy. It is a mild adult-onset s...
Mutations in the gene encoding the giant skeletal muscle protein titin are associated with a variety...
International audienceBackground and purposeThe aim was to determine the genetic background of unkno...