TGFA: exon-intron structure and evaluation as a candidate gene for Alström syndrome

Clin Genet. 1999 Jan;55(1):61-2. doi: 10.1034/j.1399-0004.1999.550111.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Chromosomes, Human, Pair 2 / genetics
  • DNA Primers
  • Diabetes Mellitus, Type 2 / genetics
  • Gene Library
  • Hearing Loss, Sensorineural / genetics
  • Humans
  • Kidney Diseases / genetics
  • Obesity / genetics
  • Retinitis Pigmentosa / genetics
  • Syndrome
  • Transforming Growth Factor alpha / genetics*

Substances

  • DNA Primers
  • Transforming Growth Factor alpha