Tuberous sclerosis. The persistent challenge of clinical diagnosis

Arch Dermatol. 1995 Dec;131(12):1460-2. doi: 10.1001/archderm.131.12.1460.
No abstract available

Publication types

  • Comment
  • Editorial

MeSH terms

  • Adult
  • Child
  • Chromosome Deletion
  • Chromosomes, Human, Pair 16
  • Chromosomes, Human, Pair 9
  • Fibroma / diagnosis
  • Fibroma / genetics
  • GTP Phosphohydrolases / genetics
  • GTPase-Activating Proteins
  • Humans
  • Infant
  • Mosaicism / genetics
  • Mutation / genetics
  • Nail Diseases / diagnosis
  • Nail Diseases / genetics
  • Phenotype
  • Proteins / genetics
  • Tuberous Sclerosis / diagnosis*
  • Tuberous Sclerosis / genetics

Substances

  • GTPase-Activating Proteins
  • Proteins
  • GTP Phosphohydrolases